Medical Device Recalls
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1 result found
510(K) Number: K981137 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic. | 2 | 07/01/2015 | BioMerieux SA |
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