Philips Healthcare Informatics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Healthcare Informatics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IntelliSpace Radiology
2
Total
2
Cleared
0
Denied
Philips Healthcare Informatics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Foster City, US.
Historical record: 2 cleared submissions from 2011 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Philips Healthcare Informatics, 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 Informatics, Inc.
2 devices