Medical Device Manufacturer · US , Andover , MA

Philips Healthcare Group - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012
1
Total
1
Cleared
0
Denied

Philips Healthcare Group has 1 FDA 510(k) cleared medical devices. Based in Andover, US.

Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Philips Healthcare Group Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Philips Healthcare Group
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