Medical Device Recalls
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1 result found
510(K) Number: K112818 |
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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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VIDAS D-Dimer Exclusion II, an automated quantitative test for use on instruments of the VIDAS famil... | 2 | 08/14/2014 | BioMerieux SA |
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