Medical Device Recalls
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1 result found
510(K) Number: K101946 |
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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 TOXO IgG Avidity is an automated qualitative test for use on the VIDAS family instruments, for... | 2 | 06/12/2018 | BioMerieux SA |
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