Ge Vingmed Ultrasound AS is one of 19 FDA 510(k) medical device manufacturers from Norway in the dataset, ranked by real submission volume.
Ge Vingmed Ultrasound AS - FDA 510(k) Cleared Devices
Recent clearances: Vivid E80 Diagnostic Ultrasound Imaging System, Vivid E90 Diagnostic Ultrasound Imaging System, Vivid E95 Diagnostic Ultrasound Imaging System, GE EchoPAC, 6VT-D ULTRASOUND TRANSDUCER
10
Total
10
Cleared
0
Denied
Ge Vingmed Ultrasound AS has 10 FDA 510(k) cleared radiology devices. Based in Horten, NO.
Historical record: 10 cleared submissions from 2009 to 2015.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC and GE Healthcare.
FDA 510(k) Regulatory Record - Ge Vingmed Ultrasound AS
10 devices
Cleared
Mar 04, 2015
Vivid E80 Diagnostic Ultrasound Imaging System, Vivid E90 Diagnostic...
Radiology
48d
Cleared
Mar 02, 2015
GE EchoPAC
Radiology
46d
Cleared
May 15, 2014
6VT-D ULTRASOUND TRANSDUCER
Radiology
17d
Cleared
Sep 24, 2013
GE ECHOPAC
Radiology
106d
Cleared
Jul 12, 2013
GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
Radiology
45d
Cleared
Jan 29, 2013
GE ECHOPAC
Radiology
42d
Cleared
Apr 19, 2012
GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
Radiology
87d
Cleared
Oct 13, 2010
GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
Radiology
173d
Cleared
Oct 05, 2010
GE ECHOPAC MODEL BT10
Radiology
147d
Cleared
Sep 28, 2009
GE VSCAN COMPACT DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
19d