Allergan Medical Optics

Allergan Medical Optics — FDA 510(k) Submissions

Allergan Medical Optics has submitted 7 FDA 510(k) premarket notifications since 1989, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Phacofragmentation, Lens, Guide, Intraocular, Forceps, Ophthalmic, Instrument, Vitreous Aspiration And Cutting, Ac-powered . Use the specialty filter in the sidebar to narrow results.