MGA-IR SIDESTREAM PCO2 MODULE

MGA-IR SIDESTREAM PCO2 MODULE is an FDA 510(k)-cleared medical device (K904863) manufactured by Marquette Gas Analysis 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 June 18, 1991. Regulation: 8.