Atlas FDA

CCY

1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Zimmerman (Spectrophotometric), 17-Ketosteroids
Device class
Class I (low risk)
Regulation
21 CFR 862.1430
Medical specialty
Clinical Chemistry
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RecordFirmDate
KETOSTEROID TEST, HYCEL-17 (K782116)Hycel, Inc.1979-01-26

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