ARROW M.I.S. MULTI-LUMEN CATHETERIZA

ARROW M.I.S. MULTI-LUMEN CATHETERIZA is an FDA 510(k)-cleared medical device (K820648) manufactured by Arrow Intl., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 13, 1982. Regulation: 8.