Gynesonics, Inc.

Gynesonics, Inc. — FDA 510(k) Submissions

Gynesonics, Inc. has submitted 8 FDA 510(k) premarket notifications since 2006, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Coagulator-cutter, Endoscopic, Unipolar (and Accessories), Transducer, Ultrasonic, Diagnostic . Use the specialty filter in the sidebar to narrow results.