Alcon Laboratories

Alcon Laboratories — FDA 510(k) Submissions

Alcon Laboratories has submitted 47 FDA 510(k) premarket notifications since 1976, of which 47 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accessories, Soft Lens Products, Unit, Phacofragmentation, Powered Laser Surgical Instrument, Case, Contact Lens, Lens, Guide, Intraocular . Use the specialty filter in the sidebar to narrow results.