Medical Device Recalls
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1 result found
510(K) Number: K023889 |
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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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| Wiener Lab CHAGATEST ELISA RECOMBINANTE V. 3.0 Diagnosis of Chagas disease. | 2 | 03/07/2018 |
FEI # 3001026625 Wiener Laboratories |
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