Medical Device Manufacturer · US , Kansas City , MO

Cerner Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1996

Total

Cleared

Denied

Cerner Corp. has 7 FDA 510(k) cleared medical devices. Based in Kansas City, US.

Historical record: 7 cleared submissions from 1996 to 2012. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Cerner Corp. Filter by specialty or product code using the sidebar.

Cerner Corp. is one of 20454 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cerner Corp.

7 devices

1-7 of 7