Meridian AG

Meridian AG — FDA 510(k) Submissions

Meridian AG has submitted 6 FDA 510(k) premarket notifications since 2002, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laser, Ophthalmic, Powered Laser Surgical Instrument, Laser, Neodymium:yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla . Use the specialty filter in the sidebar to narrow results.