VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA

VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA is an FDA 510(k)-cleared medical device (K932411) 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 September 18, 1994. Regulation: 8.