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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 25 Results
ProductCode: IYN Applicant: GENERAL ELECTRIC CO Decision Date To: 02/23/2017
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ge vivid 7, model fc0003xx GENERAL ELECTRIC CO. K031663 06/09/2003
ge vivid 7 model fc008xx, ge vivid 7 model fc009xx GENERAL ELECTRIC CO. K060542 03/31/2006
ge vivid 7 bt04 GENERAL ELECTRIC CO. K041552 07/02/2004
ge vivid 3 expert; ge vivid 3 pro GENERAL ELECTRIC CO. K020789 04/04/2002
ge vivid - i GENERAL ELECTRIC CO. K061525 07/03/2006
ge marlin ultrasound GENERAL ELECTRIC CO. K033139 10/23/2003
ge logiq twin GENERAL ELECTRIC CO. K050126 02/02/2005
ge logiq p6 GENERAL ELECTRIC CO. K073297 12/18/2007
ge logiq p5 and a5 GENERAL ELECTRIC CO. K060993 05/03/2006
ge logiq i comapact ultrasound, ge logiq e compact ultrasound, ge vivid e compact ultrasound GENERAL ELECTRIC CO. K072797 10/17/2007
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