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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 25 Results
ProductCode: IYN Applicant: GENERAL ELECTRIC CO Decision Date To: 05/23/2015
 
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ge vivid e9 ultrasound GENERAL ELECTRIC CO. K081921 08/06/2008
ge logiq p6 GENERAL ELECTRIC CO. K073297 12/18/2007
ge logiq i comapact ultrasound, ge logiq e compact ultrasound, ge vivid e compact ultrasound GENERAL ELECTRIC CO. K072797 10/17/2007
modification to ge logiq a3 GENERAL ELECTRIC CO. K072075 08/29/2007
ge vivid s5 and s6 diagnostic ultrasound GENERAL ELECTRIC CO. K071985 08/17/2007
ge voluson e8 ultrasound system GENERAL ELECTRIC CO. K061682 07/12/2006
ge vivid - i GENERAL ELECTRIC CO. K061525 07/03/2006
ge logiq 9, models 2188900, 2375600, 2404587 and 5150000 GENERAL ELECTRIC CO. K061129 06/01/2006
ge logiq p5 and a5 GENERAL ELECTRIC CO. K060993 05/03/2006
ge vivid 7 model fc008xx, ge vivid 7 model fc009xx GENERAL ELECTRIC CO. K060542 03/31/2006
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