Atlas FDA

JTM

1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Anaerobic Box Glove
Device class
Class I (low risk)
Regulation
21 CFR 866.2120
Medical specialty
Microbiology
Flags
GMP exempt
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RecordFirmDate
OXIDE ANAEROBIC SYSTEM (K800430)Oxoid U.S.A., Inc.1980-04-02

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