VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST.

VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST. is an FDA 510(k)-cleared medical device (K921201) 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 20, 1992. Regulation: 8.