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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K962695
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Product Description
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Recall
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FDA Recall
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Port-A-Cath II Polysulfone/Titanium Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm... 2 07/20/2004 Deltec, Inc
Port-A-Cath II Low Profile Polysulfone/Titanium Venous Access System, with PolyFlow Polyurethane Cat... 2 07/20/2004 Deltec, Inc
Port-A-Cath II Fluoro-Free Low Profile Venous Access System, with PolyFlow Polyurethane Catheter, 2.... 2 07/20/2004 Deltec, Inc
Port-A-Cath II Low Profile Polysulfone/Titanium Venous Access System, with PolyFlow Polyurethane Cat... 2 07/20/2004 Deltec, Inc
Port-A-Cath II Low Profile Polysulfone/Titanium Venous Access System, Pre-assembled with PolyFlow Po... 2 07/20/2004 Deltec, Inc
Port-A-Cath II Low Profile Polysulfone/Titanium Venous Access System, Pre-assembled with PolyFlow Po... 2 07/20/2004 Deltec, Inc
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