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Test ID: FHPP2    
Hypersensitivity Pneumonitis FEIA Panel II

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 manufacturer's 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.

This test was developed and its performance characteristics determined by Viracor-IBT Laboratories. It has not been cleared or approved by the FDA.

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.

86001 x 8

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

Result IDReporting NameLOINC Code
Z3166Alternaria tenuis/alternata IgGIn Process
Z3167Aspergillus fumigatus IgGIn Process
Z3168Aureobasidium pullulans IgGIn Process
Z3169Micropolyspora faeni IgGIn Process
Z3170Penicillium Chrysogenum IgGIn Process
Z3171Phoma betae IgGIn Process
Z3172Thermoactinomyces vulgaris IgGIn Process
Z3173Trichoderma viride IgGIn Process