MICRUS GUIDE WIRE, WATUSI 0.014

MICRUS GUIDE WIRE, WATUSI 0.014 is an FDA 510(k)-cleared medical device (K053265) 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 April 27, 2006. Regulation: 8.