Philips Medical Systems GmbH, Dmc is one of 25202 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Medical Systems GmbH, Dmc - FDA 510(k) Cleared Devices
Recent clearances: PHILIPS ESSENTA DR
1
Total
1
Cleared
0
Denied
Philips Medical Systems GmbH, Dmc has 1 FDA 510(k) cleared medical devices. Based in Bothell, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Philips Medical Systems GmbH, Dmc 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 Medical Systems GmbH, Dmc
1 devices