Medical Device Recalls
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1 result found
510(K) Number: K112177 |
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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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Quidel, Sofia Influenza A + B FIA, Kit #20218 (25-Test Kit), in vitro diagnostic. | 2 | 02/14/2013 | Quidel Corporation |
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