CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITE

CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITE is an FDA 510(k)-cleared medical device (K873894) manufactured by Travenol Laboratories, S.A.. 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 November 4, 1987. Regulation: 8.