Atlas FDA

FAL

1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Panendoscope (Urethroscope)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Medical specialty
Gastroenterology, Urology
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RecordFirmDate
ENDOSCOPE, UROLOGICAL, FEMALE (K770943)C.R. Bard, Inc.1977-10-18

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Every clearance here is in the API, with alerts when new ones post.