Medical Device Recalls
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1 result found
510(K) Number: K013249 |
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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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COBAS INTEGRA 400 plus analyzer used in the following assays: a)Tina-quant Apolipoprotein A-1 ver.2... | 2 | 04/10/2019 | Roche Diagnostics Corporation |
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