Medical Device Recalls
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1 result found
510(K) Number: K140377 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identif... | 2 | 06/10/2019 | Luminex Molecular Diagnostics |
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