Frigitronics of Connecticut, Inc.

Frigitronics of Connecticut, Inc. — FDA 510(k) Submissions

Frigitronics of Connecticut, Inc. has submitted 9 FDA 510(k) premarket notifications since 1976, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Cryosurgical, Accessories, Instrument, Vitreous Aspiration And Cutting, Ac-powered, Instrument, Vitreous Aspiration And Cutting, Battery-powered, Unit, Phacofragmentation . Use the specialty filter in the sidebar to narrow results.