OXYGEN MONITOR 140/141

OXYGEN MONITOR 140/141 is an FDA 510(k)-cleared medical device (K812040) manufactured by Medix Medical Electronics (U.S.A.), 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 September 20, 1981. Regulation: 8.