Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K926011 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Implantable Vascular Access System -- Infusion Ports with Silicone Rubber Catheter. Latex-Free A ... | 2 | 12/19/2006 | Arrow International Inc |
Implantable Vascular Access system --Infusion Ports with Silicone Rubber Catheter. Latex-free A P... | 2 | 12/19/2006 | Arrow International Inc |
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