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 Implantable Vascular Access System - Titanium Mini-Port with PASV Valve and 8F Silicone Cathe... | 2 | 03/15/2007 | Boston Scientific Corp |
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