Cooper Medical Devices Corp.

Cooper Medical Devices Corp. — FDA 510(k) Submissions

Cooper Medical Devices Corp. has submitted 7 FDA 510(k) premarket notifications since 1979, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Lens, Fundus, Hruby, Diagnostic, Instrument, Vitreous Aspiration And Cutting, Battery-powered, System, Abortion, Vacuum, Cannula, Ophthalmic, Instrument, Vitreous Aspiration And Cutting, Ac-powered . Use the specialty filter in the sidebar to narrow results.