MOBILE PAK, MODEL AC

MOBILE PAK, MODEL AC is an FDA 510(k)-cleared medical device (K880261) manufactured by Intl. Biomedical Concepts, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 11, 1988. Regulation: 8.