Atlas FDA

CIY

1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Radioimmunoassay, Androsterone
Device class
Class I (low risk)
Regulation
21 CFR 862.1080
Medical specialty
Clinical Chemistry
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RecordFirmDate
DHEA TEST SET (K771793)Wien Laboratories, Inc.1977-11-02

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