TRAVENOL RECONSTITUTION DEVICE W/ADMIX CAP

TRAVENOL RECONSTITUTION DEVICE W/ADMIX CAP is an FDA 510(k)-cleared medical device (K844340) 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 January 8, 1985. Regulation: 8.