American Medical Mfg., Inc.

American Medical Mfg., Inc. — FDA 510(k) Submissions

American Medical Mfg., Inc. has submitted 6 FDA 510(k) premarket notifications since 1992, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Surgical, Disposable, Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days, Marker, Skin, Light, Surgical, Accessories, Accessory, Surgical Apparel . Use the specialty filter in the sidebar to narrow results.