Medical Device Recalls
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1 result found
510(K) Number: K172868 |
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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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| Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive Protein Reagent is intended... | 2 | 12/12/2019 |
FEI # 3002808340 The Binding Site Group, Ltd. |
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