Gn Otometrics

Gn Otometrics — FDA 510(k) Submissions

Gn Otometrics has submitted 8 FDA 510(k) premarket notifications since 2008, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Auditory, Evoked Response, Nystagmograph, Audiometer, Calibrator, Hearing Aid / Earphone And Analysis Systems, Tester, Auditory Impedance . Use the specialty filter in the sidebar to narrow results.