Luneau Laboratories

Luneau Laboratories — FDA 510(k) Submissions

Luneau Laboratories has submitted 5 FDA 510(k) premarket notifications since 1984, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stand, Instrument, Ac-powered, Ophthalmic, Rack, Skiascopic, Tester, Color Vision, Curette, Uterine . Use the specialty filter in the sidebar to narrow results.