Sharn, Inc.

Sharn, Inc. — FDA 510(k) Submissions

Sharn, Inc. has submitted 4 FDA 510(k) premarket notifications since 1986, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Applicator (laryngo-tracheal), Topical Anesthesia, Stethoscope, Esophageal, Airway, Esophageal (obturator), Support, Patient Position . Use the specialty filter in the sidebar to narrow results.