Applied Medical Technology, Inc.

Applied Medical Technology, Inc. — FDA 510(k) Submissions

Applied Medical Technology, Inc. has submitted 25 FDA 510(k) premarket notifications since 1998, of which 18 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tubes, Gastrointestinal (and Accessories), Tube, Gastro-enterostomy, Enteral Specific Transition Connectors, Catheter, Suprapubic (and Accessories), Laparoscope, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.