Medical Device Recalls
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1 result found
510(K) Number: K884494 |
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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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Sheath Obturator, introducer, catheter. Obturator Accessory Kit Reorder number 406405, a 6 Fr, 15 c... | 3 | 11/03/2005 | St. Jude Medical / Daig Division |
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