SURGICAL VESSEL DILATORS-CATHERIZA-

SURGICAL VESSEL DILATORS-CATHERIZA- is an FDA 510(k)-cleared medical device (K833676) manufactured by Cimed Intl., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 1984. Regulation: 8.