B&B Medical Technologies, Inc.

B&B Medical Technologies, Inc. — FDA 510(k) Submissions

B&B Medical Technologies, Inc. has submitted 23 FDA 510(k) premarket notifications since 1986, of which 22 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Fixation, Tracheal Tube, Nebulizer (direct Patient Interface), Connector, Airway (extension), Tube, Tracheal (w/wo Connector), Flowmeter, Calibration, Gas . Use the specialty filter in the sidebar to narrow results.