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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K913459
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Product Description
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ETEST OXACILLIN OX 256 US F100 In vitro diagnostic, a quantitative technique for determining ... 2 12/19/2017 BioMerieux SA
ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic, a quantitative technique for determining th... 2 12/19/2017 BioMerieux SA
ETEST Cephalotin CE 256 Foam packaging, Product Name: ETEST Cephalothin CE 0.016-256. ETEST is a qu... 2 03/21/2017 BioMerieux SA
ETEST Gentamicin GM256 FOAM packaging, Product Name: ETEST Gentamicin GM 0.016-256(low). ETEST is a... 2 03/21/2017 BioMerieux SA
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