Philips Medical Systems North America Co. - FDA 510(k) Cleared Devices
Recent clearances: EP NAVIGATOR R3, WIRELESS PORTABLE DETECTOR FD-W17, VERADIUS, MODEL 718-130
24
Total
24
Cleared
0
Denied
FDA 510(k) Regulatory Record - Philips Medical Systems North America Co. Anesthesiology ✕
1 devices