TRAVENOL MULTIDAY INFUSOR 2C1080

TRAVENOL MULTIDAY INFUSOR 2C1080 is an FDA 510(k)-cleared medical device (K842905) 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 October 31, 1985. Regulation: 8.