CORDIS HYDRONOL STEERABLE GUIDEWIRE

CORDIS HYDRONOL STEERABLE GUIDEWIRE is an FDA 510(k)-cleared medical device (K973845) 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 January 4, 1998. Regulation: 8.