Medical Device Manufacturer · NO , Horten

Ge Vingmed Ultrasound AS - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2009
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.

FDA 510(k) Regulatory Record - Ge Vingmed Ultrasound AS
10 devices
1-10 of 10
Cleared Mar 04, 2015
Vivid E80 Diagnostic Ultrasound Imaging System, Vivid E90 Diagnostic...
K150087 · IYN
Radiology · 48d
Cleared Mar 02, 2015
GE EchoPAC
K150085 · LLZ
Radiology · 46d
Cleared May 15, 2014
6VT-D ULTRASOUND TRANSDUCER
K141093 · ITX
Radiology · 17d
Cleared Sep 24, 2013
GE ECHOPAC
K131685 · LLZ
Radiology · 106d
Cleared Jul 12, 2013
GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
K131514 · IYN
Radiology · 45d
Cleared Jan 29, 2013
GE ECHOPAC
K123894 · LLZ
Radiology · 42d
Cleared Apr 19, 2012
GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
K120201 · IYO
Radiology · 87d
Cleared Oct 13, 2010
GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
K101149 · IYO
Radiology · 173d
Cleared Oct 05, 2010
GE ECHOPAC MODEL BT10
K101324 · LLZ
Radiology · 147d
Cleared Sep 28, 2009
GE VSCAN COMPACT DIAGNOSTIC ULTRASOUND SYSTEM
K092756 · ITX
Radiology · 19d
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