PORT-A-CATH II TRANS-ARTERIAL PERCUTANEOUS SYSTEM

PORT-A-CATH II TRANS-ARTERIAL PERCUTANEOUS SYSTEM is an FDA 510(k)-cleared medical device (K992697) manufactured by Sims Deltec, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 17, 1999. Regulation: 8.