Cerner Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
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.
7 devices
Cleared
Oct 09, 2012
CERNER FETALINK+(VERSION1.0)
Obstetrics & Gynecology
116d
Cleared
Nov 27, 2009
CERNER CAREAWARE IBUS
Cardiovascular
53d
Cleared
Aug 25, 2009
CERNER FETALINK (VERSION 1.0)
Obstetrics & Gynecology
118d
Cleared
Jun 22, 2009
CERNER PROVISION WORKSTATION (VERSION 2.5)
Radiology
73d
Cleared
Mar 27, 2007
CERNER PROVISION WORKSTATION
Radiology
46d
Cleared
May 16, 2000
PROVIEW MEDICAL IMAGE DISPLAY MODULE
Radiology
68d
Cleared
Jan 26, 1996
REMOTE VIEWING SYSTEM MEDICAL IMAGE DISPLAY MODULE
Radiology
86d