Interventional technology developer Vascular Solutions of Minneapolis has received U.S. Food and Drug Administration 510(k) clearance for its Twin-Pass dual-access catheter, the firm reported.
The Twin-Pass is a two-lumen catheter designed to be used in conjunction with steerable guidewires to access discrete regions of the coronary and peripheral arterial vasculature and for use during procedures utilizing two guidewires, the company said. Vascular Solutions said it expects to launch the Twin-Pass catheter through its direct U.S. sales force next month.
By AuntMinnie.com staff writers
December 2, 2005
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