Nox Medical Ehf

Nox Medical Ehf — FDA 510(k) Submissions

Nox Medical Ehf has submitted 4 FDA 510(k) premarket notifications since 2015, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Automatic Event Detection Software For Polysomnograph With Electroencephalograph, Ventilatory Effort Recorder, Standard Polysomnograph With Electroencephalograph . Use the specialty filter in the sidebar to narrow results.