Gn Otometrics A/S

Gn Otometrics A/S — FDA 510(k) Submissions

Gn Otometrics A/S has submitted 6 FDA 510(k) premarket notifications since 2004, of which 6 received clearance as substantially equivalent to a predicate device.

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