Medical Device Recalls
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1 result found
510(K) Number: K020799 |
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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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QuickVue One-Step hCG Urine, Quidel Catalog Number: 20109, Lot Number: 706842 | 2 | 03/01/2011 | Quidel Corporation |
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