SERIES 7000 CARBON DIOXIDE MODULE

SERIES 7000 CARBON DIOXIDE MODULE is an FDA 510(k)-cleared medical device (K904789) manufactured by Marquette Electronics, 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 May 21, 1991. Regulation: 8.