Medical Device Manufacturer · US , Minneapolis , MN

Pelvital USA, Inc.

5 submissions · 5 cleared · Since 2020
5
Total
5
Cleared
0
Denied

Pelvital USA, Inc. — FDA 510(k) Submissions

Pelvital USA, Inc. has submitted 5 FDA 510(k) premarket notifications since 2020, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Perineometer . Use the specialty filter in the sidebar to narrow results.

5 devices
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All5 Gastroenterology & Urology 5