Medical Device Recalls
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1 result found
510(K) Number: K093420 |
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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 CYP2D6 Kit v3 IVD For use with Luminex 100/200 Instrument Luminex Molecular Diagnostics, Inc. 4... | 2 | 08/31/2011 | Luminex Corporation |
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