Medical Device Recalls
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1 result found
510(K) Number: K945616 |
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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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Cordis, AVANTI+ Introducer, STERILE EO, For one use only. Catalog 402656X Lot # 15076369. ... | 2 | 04/20/2010 | Cordis Corporation |
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