DRESSER ARGUS P/N 1818

DRESSER ARGUS P/N 1818 is an FDA 510(k)-cleared medical device (K905304) manufactured by Dresser Argus, 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 April 16, 1991. Regulation: 8.