Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K904334 |
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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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Ventra Percutaneous Intravenous Catheter Repair Kit for Luer Connector Segments and Single-Lumen Cat... | 2 | 07/30/2003 | Deltec, Inc |
Ventra Percutaneous Intravenous Catheter Repair Kit for 11 French Triple-Lumen External Catheter Seg... | 2 | 07/30/2003 | Deltec, Inc |
Ventra Percutaneous Intravenous Catheter Repair Kit for 9 French Dual-Lumen External Catheter Segmen... | 2 | 07/30/2003 | Deltec, Inc |
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