SCIMED(R) VENTURE(TM) II INFUSION CATHETER

SCIMED(R) VENTURE(TM) II INFUSION CATHETER is an FDA 510(k)-cleared medical device (K945904) manufactured by Scimed Peripheral Interventions. 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 18, 1995. Regulation: 8.