Philips Medizin Systeme Boeblingen GmbH

Philips Medizin Systeme Boeblingen GmbH — FDA 510(k) Submissions

Philips Medizin Systeme Boeblingen GmbH has submitted 48 FDA 510(k) premarket notifications since 2004, of which 48 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), System, Monitoring, Perinatal, Oximeter, Display, Cathode-ray Tube, Medical, System, Measurement, Blood-pressure, Non-invasive . Use the specialty filter in the sidebar to narrow results.