Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K030083 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, STD PS port, Implantable Port System, Mod... | 2 | 07/20/2004 | Boston Scientific Corporation |
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