Unicor, Inc.

Unicor, Inc. — FDA 510(k) Submissions

Unicor, Inc. has submitted 5 FDA 510(k) premarket notifications since 1995, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Set, Tubing And Support, Ventilator (w Harness), Circuit, Breathing (w Connector, Adaptor, Y Piece), Connector, Airway (extension) . Use the specialty filter in the sidebar to narrow results.