Circon Corp.

Circon Corp. — FDA 510(k) Submissions

Circon Corp. has submitted 6 FDA 510(k) premarket notifications since 1997, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Colposcope (and Colpomicroscope), Coagulator-cutter, Endoscopic, Unipolar (and Accessories), Electrode, Electrosurgical, Active, Urological, Culdoscope (and Accessories), Accessories, Catheter, G-u . Use the specialty filter in the sidebar to narrow results.