CORDIS BRITE TIP, ENVOY GUIDING CATHETER

CORDIS BRITE TIP, ENVOY GUIDING CATHETER is an FDA 510(k)-cleared medical device (K952185) 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 August 1, 1995. Regulation: 8.