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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.
82013-Acetylcholinesterase (if appropriate)
|Result ID||Reporting Name||LOINC Code|
|DAT15||EDD by US Scan||11781-2|
|6740||Last Menstrual Period (LMP)||8665-2|
|24233||EDD by LMP||11779-6|
|24239||GA at Collection by Scan||11888-5|
|24240||GA at Collection by Dates||11885-1|
|9950||Alpha Fetoprotein, AF||43798-8|
|24237||Follow up||No LOINC Needed|
|24238||General Test Info||In Process|
LOINC and CPT codes are provided by the performing laboratory.