Atlas FDA

KCM

1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Dropper, Ent
Device class
Class I (low risk)
Regulation
21 CFR 874.5220
Medical specialty
Ear, Nose, Throat
Flags
GMP exempt
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RecordFirmDate
POST-AID (K840907)E.W. Link, Inc.1984-08-02

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