C1q Complement
This assay is intended for the quantitative measurement of C1q in human serum as an aid in the diagnosis and treatment of angioedema.
ProcedureRadial immunodiffusion using calibrators referenced to CRM470. The performance characteristics of this test were determined by Eurofins Viracor. This test has been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.
7 business days from receipt of specimen
| Specimen Type | Test Code | CPT Code | NY Approved | Volume | Assay Range | Special Instructions |
|---|---|---|---|---|---|---|
| serum | 1115 | 86160 | Yes | 1 mL (min. 100 uL) |
|
2.3-23 mg/dL
Specimens are approved for testing in New York only when indicated in the Specimen Information field above.
The CPT codes provided are based on Eurofins Viracor's interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for general informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Eurofins Viracor assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.