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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K052157
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FDA Recall
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GE Innova 4100 / 4100 IQ Cardiovascular Imaging System, GE Healthcare, Waukesha, WI 53188. The pr... 2 06/19/2009 FEI # 2126677
GE Medical Systems, LLC
GE Innova 3100 / 3100 IQ Cardiovascular Imaging System, GE Healthcare, Waukesha, WI 53188. The pr... 2 06/19/2009 FEI # 2126677
GE Medical Systems, LLC
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