Phillips Medical Systems

Phillips Medical Systems — FDA 510(k) Submissions

Phillips Medical Systems has submitted 4 FDA 510(k) premarket notifications since 2004, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms), System, Imaging, Pulsed Doppler, Ultrasonic, Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms), Alarm, Blood-pressure . Use the specialty filter in the sidebar to narrow results.