Natus Manufacturing Limited

Natus Manufacturing Limited — FDA 510(k) Submissions

Natus Manufacturing Limited 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 Electrode, Needle, Diagnostic Electromyograph, Electrode, Cutaneous . Use the specialty filter in the sidebar to narrow results.