Berkeley Medevices

Berkeley Medevices — FDA 510(k) Submissions

Berkeley Medevices has submitted 5 FDA 510(k) premarket notifications since 1981, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Clamp, Surgical, General & Plastic Surgery, Retractor, Curette, Suction, Endometrial (and Accessories), System, Abortion, Vacuum, Dilator, Cervical, Hygroscopic-laminaria . Use the specialty filter in the sidebar to narrow results.