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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 25 Results
510(K) Number: K023178
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Product Description
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FDA Recall
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GE Healthcare, GE Innova 4100 / 4100 IQ. , ( The system consists of an a monoplane positioner, a va... 2 11/09/2009 GE Medical Systems, LLC
GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, ... 2 03/10/2014 GE Healthcare, LLC
GE Innova 4100 / 4100 IQ Cardiovascular Imaging System, GE Healthcare, Waukesha, WI 53188. The pr... 2 06/19/2009 GE Medical Systems, LLC
GE Innova 4100 / 4100 IQ. , GE Healthcare, Waukesha, WI 53188 ( The system consists of an a monoplan... 2 09/21/2008 GE Healthcare
GE Innova 4100 /4100 IQ. , GE Healthcare, Waukesha, WI 53188 ( The system consists of an a monoplane... 2 01/21/2009 GE Medical Systems, LLC
GE Innova 4100, GE Healthcare, Waukesha, WI 53188 ( The system consists of an a monoplane positioner... 2 09/24/2009 Ge Healthcare
GE Innova 4100-IQ, GE Healthcare, Waukesha, WI 53188 ( The system consists of an a monoplane positio... 2 09/24/2009 Ge Healthcare
Innova 4100/4100IQ system with InnovaIQ Table Option Indicated for use in generating fluoroscopi... 2 06/29/2010 Ge Healthcare, Llc
Innova 2100IQ system with InnovaIQ Table Option Indicated for use in generating fluoroscopic imag... 2 06/29/2010 Ge Healthcare, Llc
Innova 3100/ 3100IQ system with InnovaIQ Table Option Indicated for use in generating fluoroscopi... 2 06/29/2010 Ge Healthcare, Llc
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