Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K970854 |
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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 ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter | 1 | 11/09/2023 | Cordis US Corp |
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the... | 2 | 12/16/2022 | Cordis US Corp |
Cordis INFINITI 6 French Diagnostic Catheter. Catalog 534-6xxT. That is: 534614T, 534615T, 534617T... | 2 | 07/13/2006 | Cordis Corporation |
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