Medical Device Recalls
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1 result found
510(K) Number: K982315 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ProSpecT Campylobacter Microplate Assay. Catalog #2476096. | 3 | 08/17/2004 |
FEI # 1924669 Remel, Inc. |
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