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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: K113610
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BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incompatible with ANA Screen Reagent Packs/ANA Ki... 2 10/08/2021 FEI # 3008272466
Bio-Rad Laboratories, Inc.
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