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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: K233326
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Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Produc... 2 09/04/2025 FEI # 1000116130
Merge Healthcare, Inc.
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