Ni-Med, Inc.

Ni-Med, Inc. — FDA 510(k) Submissions

Ni-Med, Inc. has submitted 3 FDA 510(k) premarket notifications since 1987, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Collector, Urine, (and Accessories) For Indwelling Catheter, I.v. Start Kit, Catheters, Suction, Tracheobronchial . Use the specialty filter in the sidebar to narrow results.