MARK 4 LIQUID OXYGEN SYSTEM

MARK 4 LIQUID OXYGEN SYSTEM is an FDA 510(k)-cleared medical device (K860937) manufactured by Puritan Bennett Corp.. 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, 1986. Regulation: 8.