Path Medical GmbH

Path Medical GmbH — FDA 510(k) Submissions

Path Medical GmbH has submitted 6 FDA 510(k) premarket notifications since 2010, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Auditory, Evoked Response, Audiometer . Use the specialty filter in the sidebar to narrow results.