IRVINE, Calif.--(BUSINESS WIRE)--Reverse Medical Corporation today announced CE Mark approval, FDA 510k clearance and initial clinical use of their ReVerse® Microcatheter product line for intracranial neurovascular use. The device has been granted European Union CE Mark approval and US FDA 510k clearance for use in neuro, peripheral and coronary vasculature for the infusion of diagnostic agents such as contrast media, and therapeutic agents such as occlusion coils. This new microcatheter line also provides physicians with a steam shapeable tip option.
Help employers find you! Check out all the jobs and post your resume.
