General Electric Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
General Electric Co. - FDA 510(k) Cleared Devices
Recent clearances: GE VEO RECONSTRUCTION OPTION, GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTION, GE VIVID E9 ULTRASOUND
254
Total
254
Cleared
0
Denied
General Electric Co. has 254 FDA 510(k) cleared radiology devices. Based in Mchenry, US.
Historical record: 254 cleared submissions from 1976 to 2011.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. 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 - General Electric Co.
254 devices
Cleared
Sep 09, 2011
GE VEO RECONSTRUCTION OPTION
Radiology
287d
Cleared
Sep 26, 2008
GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTION
Radiology
44d
Cleared
Aug 06, 2008
GE VIVID E9 ULTRASOUND
Radiology
30d
Cleared
Dec 18, 2007
GE LOGIQ P6
Radiology
25d
Cleared
Nov 16, 2007
GE ECHOPAC
Radiology
29d
Cleared
Oct 17, 2007
GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E...
Radiology
16d
Cleared
Aug 29, 2007
MODIFICATION TO GE LOGIQ A3
Radiology
30d
Cleared
Aug 17, 2007
GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND
Radiology
29d
Cleared
Nov 02, 2006
GE LOGIQ WORKS
Radiology
31d
Cleared
Jul 12, 2006
GE VOLUSON E8 ULTRASOUND SYSTEM
Radiology
27d
Cleared
Jul 03, 2006
GE VIVID - I
Radiology
31d
Cleared
Jun 01, 2006
GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000
Radiology
38d
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