CORDIS VANGUARD STEERABLE GUIDEWIRES

CORDIS VANGUARD STEERABLE GUIDEWIRES is an FDA 510(k)-cleared medical device (K974560) 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 May 10, 1998. Regulation: 8.