Bip USA, Inc.

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

Bip USA, Inc. has submitted 7 FDA 510(k) premarket notifications since 1993, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Biopsy, Guide, Needle, Surgical, Device, Percutaneous, Biopsy, Instrument, Manual, Surgical, General Use, Biopsy Needle . Use the specialty filter in the sidebar to narrow results.