Ge Healthcare Information Technologies is one of 16797 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Healthcare Information Technologies - FDA 510(k) Cleared Devices
Recent clearances: CENTRICITY AW SUITE OPTION
1
Total
1
Cleared
0
Denied
Ge Healthcare Information Technologies has 1 FDA 510(k) cleared medical devices. Based in Barrington, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ge Healthcare Information Technologies 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 Information Technologies
1 devices