FLOW-I ANESTHESIA SYSTEM C20, C30 & C40

FLOW-I ANESTHESIA SYSTEM C20, C30 & C40 is an FDA 510(k)-cleared medical device (K133958) manufactured by Maquet Critical Care AB. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 2014. Regulation: 8.