MICRUS ASCENT OCCLUSION BALLOON CATHETER

MICRUS ASCENT OCCLUSION BALLOON CATHETER is an FDA 510(k)-cleared medical device (K080861) manufactured by Micrus Endovascular Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 26, 2008. Regulation: 8.