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FREMONT, Calif.--(BUSINESS WIRE)--Cordis Corporation announced the European CE marking and U.S. Food and Drug Administration (FDA) approval of additional sizes of its SLEEK® OTW platform, a 0.014 inch ultra-low profile percutaneous transluminal angioplasty (PTA) dilatation catheter. The Cordis SLEEK® OTW PTA Dilatation Catheter is a highly deliverable balloon catheter designed to treat patients undergoing peripheral angioplasty procedures below the knee. The SLEEK® OTW catheter was first launched around the world in 2011. Cordis will start commercializing these new sizes immediately in various countries around the world.
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FREMONT, Calif.--(BUSINESS WIRE)--Cordis Corporation announced the European CE marking and U.S. Food and Drug Administration (FDA) approval of additional sizes of its SLEEK® OTW platform, a 0.014 inch ultra-low profile percutaneous transluminal angioplasty (PTA) dilatation catheter. The Cordis SLEEK® OTW PTA Dilatation Catheter is a highly deliverable balloon catheter designed to treat patients undergoing peripheral angioplasty procedures below the knee. The SLEEK® OTW catheter was first launched around the world in 2011. Cordis will start commercializing these new sizes immediately in various countries around the world.
Help employers find you! Check out all the jobs and post your resume.
