Philips Medizinsysteme Boeblingen GmbH, Cardiac AN

Philips Medizinsysteme Boeblingen GmbH, Cardiac AN — FDA 510(k) Submissions

Philips Medizinsysteme Boeblingen GmbH, Cardiac AN has submitted 25 FDA 510(k) premarket notifications since 2007, of which 25 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms), Detector And Alarm, Arrhythmia, System, Monitoring, Perinatal, Oximeter, Monitor, Carbon-dioxide, Cutaneous . Use the specialty filter in the sidebar to narrow results.