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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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510(K)
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ge vivid - i GENERAL ELECTRIC CO. K061525 07/03/2006
ge vivid 3 expert; ge vivid 3 pro GENERAL ELECTRIC CO. K020789 04/04/2002
ge vivid 7 bt04 GENERAL ELECTRIC CO. K041552 07/02/2004
ge vivid 7 model fc008xx, ge vivid 7 model fc009xx GENERAL ELECTRIC CO. K060542 03/31/2006
ge vivid 7, model fc0003xx GENERAL ELECTRIC CO. K031663 06/09/2003
ge vivid e9 ultrasound GENERAL ELECTRIC CO. K081921 08/06/2008
ge vivid s5 and s6 diagnostic ultrasound GENERAL ELECTRIC CO. K071985 08/17/2007
ge voluson 730 pro/expert bt03 ultrasound system GENERAL ELECTRIC CO. K032620 10/10/2003
ge voluson 730 pro/expert untrasound bt04 GENERAL ELECTRIC CO. K041688 07/08/2004
ge voluson e8 ultrasound system GENERAL ELECTRIC CO. K061682 07/12/2006
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