Convatec, Inc.

Convatec, Inc. — FDA 510(k) Submissions

Convatec, Inc. has submitted 7 FDA 510(k) premarket notifications since 2010, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Dressing, Wound, Drug, Catheter, Straight, Pouch, Colostomy, Tubes, Gastrointestinal (and Accessories) . Use the specialty filter in the sidebar to narrow results.