Cardiopulmonary Corp.

Cardiopulmonary Corp. — FDA 510(k) Submissions

Cardiopulmonary Corp. has submitted 9 FDA 510(k) premarket notifications since 1995, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ventilator, Continuous, Facility Use, System, Network And Communication, Physiological Monitors, Accessory To Continuous Ventilator (respirator), Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) . Use the specialty filter in the sidebar to narrow results.