THERMOVENT 600, 1200, T, 02

THERMOVENT 600, 1200, T, 02 is an FDA 510(k)-cleared medical device (K874597) manufactured by Portex, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 18, 1988. Regulation: 8.