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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K012389
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FDA Recall
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GE Healthcare, Revolution XR/d. Revolution XR/d Intended Use: The Revolution XR/d Digital Radiog... 2 07/02/2014 GE Healthcare, LLC
GE Healthcare Definium 8000 Digital Radiographic Systems : GE Healthcare, 3000 North Grandview , W... 2 06/08/2012 General Electric Med Systems LLC
GE Healthcare Revolution XR/d. Model #'s 2259988-2 & 2351505. GE Healthcare, 3000 North Grandview,... 2 12/16/2009 GE Medical Systems, LLC
Revolution XR/d Wall Stand, Model Number 2291655, for Revolution XR/d Digital Radiographic Imaging S... 2 02/12/2003 General Electric Med Systems