Medical Device Recalls
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1 result found
510(K) Number: K953718 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AxSYM Digoxin II Reagent Pack, Disk Version 1. (3D53-01 or 3D53-02) The AxSYM Digoxin II assay is... | 3 | 11/21/2008 | Abbott Diagnostic International, Ltd. |
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