MEADOX SURGIMED A/S CATHETER SHEATH SYS

MEADOX SURGIMED A/S CATHETER SHEATH SYS is an FDA 510(k)-cleared medical device (K843798) manufactured by Meadox Surgimed, 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 December 26, 1984. Regulation: 8.