Philips Healthcare, Inc. is one of 16403 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Healthcare, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Philips Lumify Diagnostic Ultrasound System
1
Total
1
Cleared
0
Denied
Philips Healthcare, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bothell, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Philips Healthcare, Inc. 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, Inc.
1 devices