Medical Device Manufacturer · US , Mchenry , IL

Philips Medical Systems, Inc. - FDA 510(k) Cleared Devices

111 submissions · 110 cleared · Since 1983

Recent clearances: PCR ELEVA 1.2, PINNACLE3 SMARTARC, PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521

111
Total
110
Cleared
0
Denied

Philips Medical Systems, Inc. has 110 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 110 cleared submissions from 1983 to 2010.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Underwriters Laboratories, Inc., Entela, Inc. and Tuv Rheinland of North America, Inc..

FDA 510(k) Regulatory Record - Philips Medical Systems, Inc.

111 devices
1-12 of 111

Looking for a specific device from Philips Medical Systems, Inc.? Search by device name or K-number.

Search all Philips Medical... devices
Filters