Philips Healthcare Group is one of 16440 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Healthcare Group - FDA 510(k) Cleared Devices
Recent clearances: QLAB QUANTIFICATION SOFTWARE
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Philips Healthcare Group
1 devices