Conair Corp.

Conair Corp. — FDA 510(k) Submissions

Conair Corp. has submitted 29 FDA 510(k) premarket notifications since 1990, of which 23 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Vibrator, Therapeutic, Massager, Therapeutic, Electric, Pad, Heating, Powered . Use the specialty filter in the sidebar to narrow results.