FHLAA - Fees: HLA A High Resolution

Test Catalog

Test Name

Test ID: FHLAA    
HLA A High Resolution

Fees Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.

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Test Classification Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturers instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.

These tests were developed and their performance characteristics were determined by BloodCenter of Wisconsin. They have not been cleared by the FDA. However, this approval is not required.

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

81380

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and result codes of this test.

LOINC codes are provided by the performing laboratory.

Test IDTest Order NameOrder LOINC Value
FHLAAHLA A High Resolution57290-9

 

Result IDTest Result NameResult LOINC Value
Z0129HLA A High Resolution57290-9
Z0118Comments:48767-8

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