Ge Vingmed Ultrasound is one of 13 FDA 510(k) medical device manufacturers from Norway in the dataset, ranked by real submission volume.
Ge Vingmed Ultrasound - FDA 510(k) Cleared Devices
Recent clearances: SYSTEM FIVE/ECHOPAC WITH STRAIN RATE IMAGING
1
Total
1
Cleared
0
Denied
Ge Vingmed Ultrasound has 1 FDA 510(k) cleared medical devices. Based in Horten, NO.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ge Vingmed Ultrasound 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 Vingmed Ultrasound
1 devices