N.M. Beale Co., Inc.

N.M. Beale Co., Inc. — FDA 510(k) Submissions

N.M. Beale Co., Inc. has submitted 5 FDA 510(k) premarket notifications since 1990, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscope Channel Accessory, Applicator (laryngo-tracheal), Topical Anesthesia, Endoscopic Irrigation/suction System, Transducer, Ultrasonic, Diagnostic, Tubes, Gastrointestinal (and Accessories) . Use the specialty filter in the sidebar to narrow results.