Medical Device Recalls
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1 result found
510(K) Number: K113382 |
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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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Alfa Wassermann Diagnostic Technologies, LLC. ACE AST Reagent. Product Usage: For quantitativ... | 2 | 04/30/2014 | Alfa Wassermann, Inc. |
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