Medical Device Recalls
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1 result found
510(K) Number: K990722 |
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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 XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative techniq... | 2 | 02/21/2017 | BioMerieux SA |
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