Medical Device Recalls
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1 result found
510(K) Number: K101879 |
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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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Cepheid brand Xpert MRSA/SA-BC US-IVD, an In-vitro diagnostic test kit, Catalog Numbers: GXMRSA/SA-B... | 3 | 01/11/2012 | Cepheid |
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