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Test ID: FHPP2    
Hypersensitivity Pneumonitis FEIA Panel II

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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 order and result codes of this test.

Test IDTest Order NameOrder LOINC Code
FHPP2Hypersensitivity Pneumonitis FEIA Panel IIIn Process


Result IDTest Result NameResult LOINC Code
Z3166Alternaria tenuis/alternata IgG26951-4
Z3167Aspergillus fumigatus IgG26954-8
Z3168Aureobasidium pullulans IgG26955-5
Z3169Micropolyspora faeni IgG26948-0
Z3170Penicillium Chrysogenum IgG6212-5
Z3171Phoma betae IgG35551-1
Z3172Thermoactinomyces vulgaris IgG34190-9
Z3173Trichoderma viride IgG49687-7

LOINC and CPT codes are provided by the performing laboratory.