Ge Healthcare Integrated IT Solutions is one of 16440 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Healthcare Integrated IT Solutions - FDA 510(k) Cleared Devices
Recent clearances: CENTRICITY PACS-IW, CENTRICITY CARDIO IMAGING, CENTRICITY PERINATAL AND CENTRICITY INTENSIVE CARE
4
Total
4
Cleared
0
Denied
Ge Healthcare Integrated IT Solutions has 4 FDA 510(k) cleared medical devices. Based in Barrington, US.
Historical record: 4 cleared submissions from 2006 to 2012. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ge Healthcare Integrated IT Solutions 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 - Ge Healthcare Integrated IT Solutions
4 devices
Cleared
Jun 05, 2012
CENTRICITY PACS-IW
Radiology
28d
Cleared
Nov 30, 2011
CENTRICITY CARDIO IMAGING
Radiology
85d
Cleared
Sep 26, 2011
CENTRICITY PERINATAL AND CENTRICITY INTENSIVE CARE
Obstetrics & Gynecology
110d
Cleared
Dec 26, 2006
CENTRICITY RADIOLOGY RA600, CARDIOLOGY CA1000 AND DIGITAL HARDCOPY
Radiology
20d