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Test ID: AFPA    
Alpha-Fetoprotein, Amniotic Fluid

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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 has been cleared or approved by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

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.


82013-Acetylcholinesterase (if appropriate)

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
6739Collection Date33882-2
DAT15EDD by US ScanIn Process
6740Last Menstrual Period (LMP)8665-2
24233EDD by LMP11779-6
24239GA at Collection by Scan11888-5
24240GA at Collection by Dates11885-1
24234GA Used21299-3
9950Alpha Fetoprotein, AF43798-8
24236Additional Comments55107-7
24237Follow upIn Process
24238General Test InfoIn Process

LOINC and CPT codes are provided by the performing laboratory.