Ge Imatron is one of 25883 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Imatron - FDA 510(k) Cleared Devices
Recent clearances: E-SPEED EBT SCANNER SYSTEM
1
Total
1
Cleared
0
Denied
Ge Imatron has 1 FDA 510(k) cleared medical devices. Based in South San Fransisco, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ge Imatron Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ge Imatron
1 devices