CORDIS WIZDOM STEERABLE GUIDEWIRE

CORDIS WIZDOM STEERABLE GUIDEWIRE is an FDA 510(k)-cleared medical device (K953760) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 6, 1995. Regulation: 8.