Medical Device Recalls
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1 result found
510(K) Number: K020666 |
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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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Baxter Duploject Easy Prep, Fibrin Sealant Preparation and Application System ISO; Product Codes: 1... | 2 | 11/24/2007 | Baxter Bioscience |
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