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Test ID: FSPII    
Stachybotrys 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/Allergen specific IgG; quantitative or semiquantitative

86003/Allergen specific IgE; quantitative or semiquantitative

83520/not otherwise specified

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
FSPIIStachybotrys Panel IIIn Process


Result IDTest Result NameResult LOINC Code
Z3154Stachybotrys chartarum/atra IgEIn Process
Z3155Stachybotrys chartarum/atra IgGIn Process
Z3156Stachybotrys chartarum/atra IgAIn Process

LOINC and CPT codes are provided by the performing laboratory.