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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K023178
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Product Description
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FDA Recall
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Innova 4100 / 4100 IQ , GE Healthcare, Waukesha, WI 53188 (The system consists of an a monoplane pos... 2 09/20/2008 GE Healthcare
Innova 4100 / 4100 IQ, GE Healthcare, Waukesha, WI 53188 ( The system consists of an a monoplane pos... 2 03/12/2009 GE Medical Systems, LLC
Innova 4100/4100IQ GE Innova 4100 / 4100 IQ. , GE Healthcare, Waukesha, WI 53188 ( The system consis... 2 11/16/2010 GE Healthcare, LLC
Innova 4100/4100IQ is a X-Ray system that consists of an a monoplane positioner, a vascular or cardi... 2 09/16/2008 GE Healthcare
Omega IV and Omega V tables on GE Innova 4100/4100IQ GE Innova 4100 / 4100 IQ., x-ray system 2 01/13/2010 GE Medical Systems, LLC
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