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AV access
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FDA Indication for Viabahn Endoprosthesis for Revision of AV Access Is Expanded by Gore
Dec 13, 2013W. L. Gore & Associates (Gore) has obtained the US Food and Drug Administration (FDA) approval for its GORE VIABAHN endoprosthesis for the treatment of stenosis or thrombotic occlusion at the venous anastomosis of synthetic arteriovenous ...
Tags: Gore, FDA, GORE VIABAHN, endoprosthesis, AV access
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FDA Has Granted Approval to Cryolife's New Hemodialysis Reliable Outflow (Hero) Device
Apr 5, 2013The US Food and Drug Administration (FDA) has granted 510(k) approval to CryoLife's new Hemodialysis Reliable Outflow (HeRO) device. The device, which the company claims, is the only subcutaneous AV access solution that maintains ...
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