Cybernius Medical , Ltd.

Cybernius Medical , Ltd. — FDA 510(k) Submissions

Cybernius Medical , Ltd. has submitted 1 FDA 510(k) premarket notifications since 1997, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Dialysate Delivery, Semi-automatic, Peritoneal . Use the specialty filter in the sidebar to narrow results.