IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI

IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI is an FDA 510(k)-cleared medical device (K844937) manufactured by Y. 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 24, 1985. Regulation: 8.