CORDIS CATHETER SHEATH INTRODUCER

CORDIS CATHETER SHEATH INTRODUCER is an FDA 510(k)-cleared medical device (K932733) 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 25, 1993. Regulation: 8.