Medical Device Manufacturer · DE , Boeblingen

Philips Medizin Systeme B?blingen GmbH - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2022
8
Total
8
Cleared
0
Denied

Philips Medizin Systeme B?blingen GmbH has 8 FDA 510(k) cleared medical devices. Based in Boeblingen, DE.

Latest FDA clearance: Nov 2025. Active since 2022. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Philips Medizin Systeme B?blingen GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Philips Medizin Systeme Böblingen GmbH as regulatory consultant.

FDA 510(k) Regulatory Record - Philips Medizin Systeme B?blingen GmbH
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