SOFTECH PLUS ETC02 CANNULA

SOFTECH PLUS ETC02 CANNULA is an FDA 510(k)-cleared medical device (K132946) manufactured by Teleflexmedical, 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 June 3, 2014. Regulation: 8.