Medical Device Recalls
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1 result found
510(K) Number: K060540 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Cepheid, Xpert GBS Assay Diagnostic Test Kit Part No: GXGBS-100N-10 (in foil pouch) for use with th... | 3 | 01/12/2008 |
FEI # 3004530258 Cepheid |
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