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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 15 Results
510(K) Number: K093514
 
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Product Description
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Discovery 670 DR (Model H3100BT), NM/CT 870 DR (Model 3100Q and H3100AS), Discovery NM670 Pro (Model... 2 01/13/2021 GE Healthcare, LLC
Discovery 670 DR Model # H3100BT 2 09/21/2020 GE Healthcare, LLC
NM/CT 870 DR Model # H3100AS 2 09/21/2020 GE Healthcare, LLC
Discovery NM670 Pro Model # H3100XB 2 09/21/2020 GE Healthcare, LLC
Discovery NM/CT 670 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intend... 2 05/03/2019 GE Healthcare, LLC
NM/CT 870 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use... 2 05/03/2019 GE Healthcare, LLC
Discovery NM/CT 670 ES Product Usage: The GE Discovery NM/CT 670 system is a medical tool intende... 2 05/03/2019 GE Healthcare, LLC
Discovery NM/CT 670 ES, model 5376204-70-57 2 12/13/2018 GE Healthcare, LLC
Discovery NM/CT 670 DR, model 5376204-70-56 intended for use in detecting, localizing, diagnosing o... 2 12/13/2018 GE Healthcare, LLC
Discovery NM/CT 670 Pro, model 5376204-70-54 2 12/13/2018 GE Healthcare, LLC
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