Medical Device Recalls
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1 result found
510(K) Number: K163626 |
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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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Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452 | 2 | 08/15/2019 | Luminex Corporation |
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