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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K022322
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FDA Recall
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Innova 2000 2 12/23/2016 FEI # 2126677
GE Healthcare, LLC
GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova 2000S mobile version. C... 2 05/24/2006 FEI # 2126677
GE Healthcare
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