Philips Medizin Systeme is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Philips Medizin Systeme - FDA 510(k) Cleared Devices
Recent clearances: Nasal Alar SpO2 Sensor (989803205381)
1
Total
1
Cleared
0
Denied
Philips Medizin Systeme has 1 FDA 510(k) cleared medical devices. Based in Boblingen, DE.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Philips Medizin Systeme Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips Medizin Systeme
1 devices