Vios Medical, Inc.

Vios Medical, Inc. — FDA 510(k) Submissions

Vios Medical, Inc. has submitted 3 FDA 510(k) premarket notifications since 2015, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm), Display, Cathode-ray Tube, Medical . Use the specialty filter in the sidebar to narrow results.