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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K202966
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SIGNA Architect, with affected software versions: DV26.0 to DV26.3, DV27.0 to DV27.3, DV28.0 to DV2... 2 08/02/2024 FEI # 2183553
GE Medical Systems, LLC
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