Philips Nuclear Medicine, Inc. is one of 21587 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Nuclear Medicine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NM APPLICATION SUITE
1
Total
1
Cleared
0
Denied
Philips Nuclear Medicine, Inc. has 1 FDA 510(k) cleared medical devices. Based in Milpitas, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Philips Nuclear Medicine, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Philips Nuclear Medicine, Inc.
1 devices