CORDIS AVANTI TRANS-RADIAL CATHETER SHEATH INTRODUCER KIT

CORDIS AVANTI TRANS-RADIAL CATHETER SHEATH INTRODUCER KIT is an FDA 510(k)-cleared medical device (K962746) 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 October 10, 1996. Regulation: 8.