F. & F. Koenigkramer

F. & F. Koenigkramer — FDA 510(k) Submissions

F. & F. Koenigkramer has submitted 9 FDA 510(k) premarket notifications since 1977, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Chair, Ophthalmic, Ac-powered, Stand, Instrument, Ac-powered, Ophthalmic, Remover, Intrauterine Device, Contraceptive, Hook-type, Laser, Ophthalmic, Unit, Examining/treatment, Ent . Use the specialty filter in the sidebar to narrow results.