Physio-Control, Inc.

Physio-Control, Inc. — FDA 510(k) Submissions

Physio-Control, Inc. has submitted 14 FDA 510(k) premarket notifications since 1984, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Automated External Defibrillators (non-wearable), System, Network And Communication, Physiological Monitors, Dc-defibrillator, Low-energy, (including Paddles), Auxiliary Power Supply (ac Or Dc) For Low-energy Dc-defibrillator, Aid, Cardiopulmonary Resuscitation . Use the specialty filter in the sidebar to narrow results.