Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K974471 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen Pol... | 2 | 07/20/2004 |
FEI # 2183502 Deltec, Inc |
| Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen Pol... | 2 | 07/20/2004 |
FEI # 2183502 Deltec, Inc |
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