Medical Device Recalls
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1 result found
510(K) Number: K760318 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dade Actin Activated Cephaloplastin Reagent; Liquid rabbit brain cephalin with plasma activator for ... | 2 | 06/02/2015 | Siemens Healthcare Diagnostics, Inc. |
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