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Ordering information regarding a HPV Assay Test for Clinical Diagnostic Laboratories. Human Papillomavirus (HPV), High Risk with 16 and 18 Genotype by Liquid-Based Pap Test and Hologic Thin Prep Ordering Recommendation This FDA-approved test and platform is designed for primary HPV screening in individuals aged 25 and older with a cervix. It is also FDA-approved for routine cervical cancer screening in combination with cervical cytology (Pap smear) for those aged 30 and older. Additionally, it serves as a follow-up test for abnormal cytology results in individuals aged 21 and older. Mnemonic Methodology Qualitative Polymerase Chain Reaction Performed Mon-Sat Reported Within 1-5 days Specimen Required Patient Preparation: Collect: Cervical, anal, or vaginal specimen with brush or spatula from ThinPrep kit and place in PreservCyt Media Specimen Preparation: Mix well. Transfer 3 mL to a Standard Transport Tube. (Min 1.5 mL). For primary screening purposes, please submit a specimen aliquot and keep the original specimen at the client site. Storage/Transport Temperature: Refrigerated Unacceptable Conditions: Bloody or dark brown specimens. Specimens in any media other than indicated above. Remarks: Specimen source required. Stability: Ambient: 6 months; Refrigerated: 6 months; Frozen: Unacceptable Reference Interval Negative Interpretive Data This test detects the DNA of HPV16, HPV18, and 12 other high-risk HPV types (31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68) that are linked to cervical cancer and its precursor lesions. The accuracy of the results may be influenced by specimen collection methods, the infection stage, and the presence of interfering substances. It's crucial to interpret these results alongside other laboratory and clinical data. A negative high-risk HPV result does not rule out the presence of other high-risk HPV types, potential future cytologic abnormalities, underlying CIN2-3, or cancer. HPV testing is not recommended for the screening or management of atypical squamous cells of undetermined significance (ASCUS) in women under 21 years of age. Note CPT Code 87624 Components Component Chart Name Component Test Code LOINC HPV Source 0060752 31208-2 2011935 HPV Genotype 16 by PCR 77399-4 2011936 2011941 HPV, Other High Risk by PCR 82675-0 HPV Genotype 18 by PCR 77400-0 Aliases HPV High Risk HPV HR ThinPrep HPV Primary screening Human papilloma virus

We Provide Services for a Wide Variety of Companies and Organizations At our Medical Laboratory, we offer comprehensive services for companies and organizations. We provide a wide variety of medical testing, including drug screening for new employees, blood tests, and COVID or FLU testing for travel purposes. Our highly experienced team is capable of accommodating large groups efficiently and effectively. Contact us today for more information Contact Us Learn More Learn More Learn More Learn More Services for Life Insurance Companies Learn More Services for Government Agencies Learn More Services for Employer Solutions Learn More Services for Employer Solutions Learn More

Ordering information regarding a T- Uptake test for Clinical Diagnostic Laboratories. Thyroxine, Free (Free T4) Ordering Recommendation The preferred alternative to this test is Thyroxine, Free (Free T4) Methodology Quantitative Electrochemiluminescent Immunoassay (ECLIA) Performed Mon-Sat Reported Within 24 hours New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube or plasma separator tube. Also acceptable: Green (lithium heparin), lavender Specimen Preparation: Allow specimen to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 2 hours of collection. Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Grossly hemolyzed specimens. Remarks: Stability: After separation of cells: Ambient: 8 days; Refrigerated: 2 weeks; Frozen: 2 years Reference Interval Free Thyroxine, ng/dL 0-3 days 0.7-2.7 ng/dL 4-30 days 0.8-3.1 ng/dL 1-23 months 2-6 years 0.5-2.3 ng/dL 0.9-1.8 ng/dL 7-11 years 0.9-1.7 ng/dL 12-19 years 12-19 years 0.9-1.6 ng/dL 0.9-1.6 ng/dL 20 years and older 0.9-1.7 ng/dL Pregnancy, 1st Trimester 0.9-1.4 ng/dL Pregnancy, 2nd Trimester 0.7-1.3 ng/dL Interpretive Data Thyroxine, Free (Free T4) is the preferred test alternative for T Uptake and Free Thyroxine Index tests. Note CPT Code 84439 Components Component Test Code Component Chart Name LOINC 0070138 Thyroxine Free 3024-7 Aliases Free Thyroxine FT4, Serum Non-Protein Bound Tetraiodothyronine T4 Free, Serum T4, Free Thyroid Function Cascade

The product page for the men's health panel at Clinical Diagnostic Laboratories. Men's Health Panel Take charge of your health with this comprehensive blood test panel designed specifically for men. Whether you're focused on energy levels, heart health, hormone balance, or just getting a clearer picture of your overall wellness, this panel covers the essentials. Here’s what it checks — and why it matters: Complete Blood Count (CBC) – Measures your white and red blood cells to detect signs of infection, fatigue, or anemia. Comprehensive Metabolic Panel (CMP) – Evaluates your liver and kidney function, electrolytes, and blood sugar levels. Lipid Panel – Checks your cholesterol, including “good” (HDL) and “bad” (LDL) cholesterol, to assess your heart disease risk. Testosterone, Total – Measures your testosterone levels, which impact energy, muscle mass, mood, and sexual health. PSA, Total – Screens for signs of prostate issues, which is especially important as men age. Recommended for men over 50. Hemoglobin A1C – Provides a long-term view of your blood sugar levels to check for prediabetes or diabetes. Vitamin B12 – Plays a crucial role in the formation of red blood cells, the synthesis of DNA, and the maintenance of nerve cells. TSH (Thyroid-Stimulating Hormone) – Helps detect thyroid issues that can affect metabolism, weight, and energy. With just one visit to our lab, you’ll gain valuable insight into your health — without needing a doctor’s referral or insurance. $241.00 Taxes will be calculated at checkout Buy Now

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Ordering information regarding a T4 Total test for Clinical Diagnostic Laboratories. Thyroxine, Total T4 (Total T4) Ordering Recommendation Preferred test for initial screening and monitoring of thyroid function. Methodology Quantitative Electrochemiluminescent Immunoassay (ECLIA) Performed Mon-Sat Reported Within 24 hours New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube or green (lithium heparin). Also acceptable: lavender Specimen Preparation: Separate serum or plasma from cells ASAP or within 2 hours of collection. Allow serum specimen to clot completely at room temperature. Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Grossly hemolyzed specimens. Remarks: Stability: After separation from cells: Ambient: 4 days; Refrigerated: 8 days; Frozen: 1 year Reference Interval Components Available Separately Reference Interval Thyroxine, Total T4 Cord Blood 6.60-17.50 ug/dL 0-3 days 5.37-22.40 ug/dL 4-30 days 5.24-23.20 ug/dL 1-23 months 5.37-16.00 ug/dL 2-6 years 5.26-14.80 ug/dL 7-11 years 5.70-14.10 ug/dL 12-19 years 4.74-14.60 ug/dL 20 years and older 4.50-11.70 ug/dL Interpretive Data Note CPT Code 84436 Components Component Test Code Component Chart Name LOINC 3005980 Thyroxine, Total T4 3026-2 Aliases Syn-Thyroid T4 T4 Serum T4 Total Only Tetraiodothyronine Thyroid Hormone Thyroxine (T4) Total T4

Ordering information regarding a Serine Proteinase 3 (PR3) Antibody for Clinical Diagnostic Laboratories. Serine Proteinase 3 (PR3) Antibody Ordering Recommendation When used in conjunction with other autoantibody tests (ANCA, MPO), may aid in differentiating suspected Wegener granulomatosis (WG) from other vasculitides. May be useful to monitor patients with PR3 antibodies. Panel tests are available. For the workup of suspected vasculitis, refer to ANCA-Associated Vasculitis Profile (ANCA/MPO/PR3) (3003745 ). For patients with a history of vasculitis, refer to Myeloperoxidase (MPO) Antibody and Serine Proteinase 3 (PR3) Antibody with Reflex to Anti-Neutrophil Cytoplasmic Antibody, IgG by IFA (3003746 ). Mnemonic PR3 Performed Mon-Sat Methodology Semi-Quantitative Multiplex Bead Assay Reported 1-2 Days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to a Standard Transport Tube. (Min: 0.2 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Plasma, urine, or other body fluids. Contaminated, hemolyzed, or severely lipemic specimens., icteric, or lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles) Reference Interval 19 AU/mL or less Negative 20-25 AU/mL 26 AU/mL or greater Equivocal Positive Interpretive Data Approximately 85% of patients with a C-ANCA pattern by IFA have antibodies specific for PR3. Compliance Category: FDA Note CPT Code 83516 Components Component Chart Name Serine Proteinase 3 (PR3) Ab, IgG Component Test Code 0050527 LOINC 6968-2 Aliases PR3 PR3 Ab PR3 IgG Antibodies

The product page for the general Women's Health Panel Clinical Diagnostic Laboratories. Women's Health Panel Feel your best, inside and out. This comprehensive blood panel is designed specifically for women to provide a clear picture of your overall health, hormone balance, and essential nutrients. Whether you’re managing symptoms, staying proactive, or just checking in — this panel helps you take control of your wellness. Here’s what it checks — and why it matters: Complete Blood Count (CBC) – Measures your white and red blood cells to check for signs of fatigue, infection, or anemia. Comprehensive Metabolic Panel (CMP) – Evaluates your liver and kidney function, blood sugar, and electrolyte balance. Lipid Panel – Assesses cholesterol levels, including “good” (HDL) and “bad” (LDL) cholesterol, to help understand your heart health. TSH (Thyroid-Stimulating Hormone) – Screens for thyroid issues that can affect weight, mood, and energy. T4, Total & T3, Free – Additional thyroid hormones that give a fuller view of thyroid function and metabolic health. Estradiol, LH, FSH – These hormones play a major role in reproductive health, menstrual cycles, fertility, and symptoms like hot flashes or irregular periods. Vitamin D – Checks for deficiency in this key vitamin that supports your bones, immune health, and mood. Ferritin – Measures iron storage in the body, which can help explain fatigue, hair thinning, or low energy. One blood draw — no referrals, no insurance required. Just clear answers, fast results, and the confidence to take control of your health. $263.50 Taxes will be calculated at checkout Buy Now

Services for Life Insurance Companies We Care About Your Applicants Clinical Diagnostics Laboratories cares about your applicants and their goal to acquire life insurance. We promise to provide your life insurance applicants with professional laboratory testing to assist in their application process that is done with dignity. We provide laboratory testing using state-of-the-art testing equipment. With the ability to gain results in 24hrs with easy scheduling options . Our highly skilled professionals are on standby to treat your applicants with the highest degree of care and efficiency. Click here today to get started. Contact Us

Ordering information regarding a Glomerular Basement Membrane Antibody test for Clinical Diagnostic Laboratories. Glomerular Basement Membrane Antibody, IgG (IFA) Ordering Recommendation May be useful in detecting glomerular basement membrane (GBM) antibodies. Combined use of IFA Glomerular Basement Membrane Antibody, IgG by Multiplex Bead Assay and IFA (2008403 ) may improve diagnostic sensitivity for disease. If positive, may be useful for monitoring treatment response. Mnemonic GBM-G IFA Performed Mon-Sat Methodology Indirect Fluorescent Antibody Reported 1-3 Days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transport 1 mL serum. (Min: 0.5 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles) Reference Interval Negative Interpretive Data When present, IgG antibody to glomerular basement membrane (GBM) antigen detected by either indirect fluorescent antibody (IFA) or multiplex bead assay helps support a diagnosis of Goodpasture syndrome. However, the combined result of both assays performed during initial evaluation improves the diagnostic sensitivity for disease. A positive result in one or both assays should be confirmed by renal biopsy. This test was developed and its performance characteristics were determined by CDL. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes. Compliance Category: FDA Note CPT Code 86255 Components Component Chart Name GBM Antibody, IgG by IFA Component Test Code 0049191 LOINC 29994-1 Aliases Anti-GBM Antibody Anti-Glomerular Basement Membrane Antibody GBM IgG IFA