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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K032399
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VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226 2 01/04/2023 FEI # 1950204
Biomerieux Inc
VITEK 2 REAGENT AST-GP75 TEST KIT 20 CARDS, CATALOG 415670 2 01/04/2023 FEI # 1950204
Biomerieux Inc
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