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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K040845
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VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS, CATALOG 413437 2 01/04/2023 FEI # 1950204
Biomerieux Inc
VITEK 2 REAGENT AST-GN69 TEST KIT 20 CARDS, CATALOG 413400 2 01/04/2023 FEI # 1950204
Biomerieux Inc
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