Philips Medical Systems B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Philips Medical Systems B.V. - FDA 510(k) Cleared Devices
Recent clearances: Azurion R3.1, Azurion R3.1
3
Total
3
Cleared
0
Denied
Philips Medical Systems B.V. has 3 FDA 510(k) cleared medical devices. Based in Best, NL.
Latest FDA clearance: Jul 2026. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Philips Medical Systems B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips Medical Systems B.V.
3 devices