CORDIS CATH SHEATH INTRODUC/MID-LENGTH SHEATH SYST

CORDIS CATH SHEATH INTRODUC/MID-LENGTH SHEATH SYST is an FDA 510(k)-cleared medical device (K861082) 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 May 4, 1986. Regulation: 8.