Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K083269 |
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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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Reinforced Catheter Introducer System, 5 per carton. The product is sold under the Cordis Crossover ... | 1 | 11/24/2009 | Thomas Medical Products Inc |
Cordis CROSSOVER. Cordis CROSSOVER Sheath Introducer. Thomas Medical Products, Inc. 65 Great Valle... | 1 | 11/05/2009 | Cordis Corporation |
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