Micromedics, Inc.

Micromedics, Inc. — FDA 510(k) Submissions

Micromedics, Inc. has submitted 29 FDA 510(k) premarket notifications since 1983, of which 29 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Syringe, Piston, Syringe, Irrigating (non Dental), Cannula, Sinus, Tube, Tympanostomy . Use the specialty filter in the sidebar to narrow results.