Medical Products Development, Inc.

Medical Products Development, Inc. — FDA 510(k) Submissions

Medical Products Development, Inc. has submitted 13 FDA 510(k) premarket notifications since 1980, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Cautery, Thermal, Battery-powered, Electrosurgical, Cutting & Coagulation & Accessories, Light, Surgical, Instrument, Apparatus, Electrosurgical, Unit, Cautery, Thermal, Ac-powered . Use the specialty filter in the sidebar to narrow results.