Aktormed GmbH

Aktormed GmbH — FDA 510(k) Submissions

Aktormed GmbH has submitted 4 FDA 510(k) premarket notifications since 2018, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Surgical, Computer Controlled Instrument, Endoscope Holder, Software Controlled Endoscope And Instrument Holder . Use the specialty filter in the sidebar to narrow results.