Neomed, Inc.

Neomed, Inc. — FDA 510(k) Submissions

Neomed, Inc. has submitted 13 FDA 510(k) premarket notifications since 2007, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Enteral Syringes With Enteral Specific Connectors, Tube, Feeding, Catheter, Umbilical Artery, Syringe, Piston, Tubes, Gastrointestinal (and Accessories) . Use the specialty filter in the sidebar to narrow results.