VITAL-PORT DUAL LUMEN VASCULAR ACCESS SYSTEM 1121

VITAL-PORT DUAL LUMEN VASCULAR ACCESS SYSTEM 1121 is an FDA 510(k)-cleared medical device (K912465) manufactured by Med Institute, 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 July 29, 1991. Regulation: 8.