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General Electric Co.

FDA 510(k) & PMA Approved Devices — 254 products

Total Devices254
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K103489 GE VEO RECONSTRUCTION OPTIONJAK2011-09-09 View
510(k) K082317 GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTIONKGI2008-09-26 View
510(k) K081921 GE VIVID E9 ULTRASOUNDIYN2008-08-06 View
510(k) K073297 GE LOGIQ P6IYN2007-12-18 View
510(k) K072952 GE ECHOPACLLZ2007-11-16 View
510(k) K072797 GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUNDIYO2007-10-17 View
510(k) K072075 MODIFICATION TO GE LOGIQ A3IYN2007-08-29 View
510(k) K071985 GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUNDIYN2007-08-17 View
510(k) K063006 GE LOGIQ WORKSLLZ2006-11-02 View
510(k) K061682 GE VOLUSON E8 ULTRASOUND SYSTEMIYO2006-07-12 View
510(k) K061525 GE VIVID - IIYN2006-07-03 View
510(k) K061129 GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000IYN2006-06-01 View
510(k) K060993 GE LOGIQ P5 AND A5IYN2006-05-03 View
510(k) K060542 GE VIVID 7 MODEL FC008XX, GE VIVID 7 MODEL FC009XXIYN2006-03-31 View
510(k) K053435 GE VOLUSON IIYN2005-12-16 View
510(k) K052441 GE LOGIQ 7 ULTRASOUND BT05IYN2005-09-21 View
510(k) K050943 GE VIEWPOINTLLZ2005-05-23 View
510(k) K050704 MODIFICATION TO: REVOLUTION XR/D DIGITAL RADIOGRAPHIC IMAGING SYSTEM WITH IMAGE PASTING AND AUTOPOSITIONINGKPR2005-04-08 View
510(k) K050126 GE LOGIQ TWINIYN2005-02-02 View
510(k) K043112 GE 0.2T SIGNA PROFILE EXCITE MR SYSTEMLNH2004-11-24 View
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