Medical Device Recalls
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1 result found
510(K) Number: K032014 |
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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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N Latex IgM; In-vitro diagnostic reagent for the quantitative determination of IgM in human cerebros... | 3 | 03/17/2015 | Siemens Healthcare Diagnostics, Inc. |
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