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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K904334
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Product Description
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Recall
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FDA Recall
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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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