Medical Device Manufacturer · GB , Nottingham, England

Femcare , Ltd.

2 submissions · 2 cleared · Since 1988
2
Total
2
Cleared
0
Denied

Femcare , Ltd. — FDA 510(k) Submissions

Femcare , Ltd. has submitted 2 FDA 510(k) premarket notifications since 1988, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Suprapubic (and Accessories), Surgical Instruments, G-u, Manual (and Accessories) . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Gastroenterology & Urology 2