Medical Device Recalls
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1 result found
510(K) Number: K142033 |
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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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| Verigene Enteric Pathogens Nucleic Acid Test (EP) for detecting and identification of pathogenic en... | 2 | 10/11/2018 |
FEI # 3002524000 Luminex Corporation |
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