Medical Device Recalls
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1 result found
510(K) Number: K954595 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Product is Cordis Brite Tip Catheter Sheath Introducer (4, 7, 8, 9, 10 and 11French sizes only). | 2 | 06/12/2003 | Cordis Corporation |
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