Biomedical Devices, Inc.

Biomedical Devices, Inc. — FDA 510(k) Submissions

Biomedical Devices, Inc. has submitted 7 FDA 510(k) premarket notifications since 1983, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Hood, Surgical, Mixer, Breathing Gases, Anesthesia Inhalation, Orthopedic Manual Surgical Instrument, Cement Obturator, Catheter, Irrigation . Use the specialty filter in the sidebar to narrow results.