Lasermatic OY

Lasermatic OY — FDA 510(k) Submissions

Lasermatic OY has submitted 2 FDA 510(k) premarket notifications since 1988, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Laser Surgical Instrument, Laser, Ent Microsurgical Carbon-dioxide . Use the specialty filter in the sidebar to narrow results.