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Test ID: FPHET
Anti-Phosphatidylethanolamine Panel

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Test ClassificationProvides 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 instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.

The performance characteristics of the listed assays were validated by BioAgilytix Diagnostics. The US FDA has not approved or cleared these tests. The results of these assays can be used for clinical diagnosis without FDA approval. BioAgilytix Diagnostics is a CLIA certified, CAP accredited laboratory for performing high complexity assays.

CPT Code InformationProvides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic 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.

83520 x 3

LOINC® InformationProvides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

Test ID Test Order Name Order LOINC Value
FPHET Anti-Phosphatidylethanolamine Panel Not Provided

Result ID Test Result Name Result LOINC ValueApplies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
Z0143 Anti-Phosphatidylethanolamine IgA 13078-1
Z0150 Anti-Phosphatidylethanolamine IgG 13076-5
Z0142 Anti-Phosphatidylethanolamine IgM 13077-3