HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT

HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT is an FDA 510(k)-cleared medical device (K953544) manufactured by Gibeck, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 24, 1995. Regulation: 8.