American Laser Corp.

American Laser Corp. — FDA 510(k) Submissions

American Laser Corp. has submitted 5 FDA 510(k) premarket notifications since 1982, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Laser Surgical Instrument, Instrument, Visual Field, Laser, Laser, Ophthalmic . Use the specialty filter in the sidebar to narrow results.