HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE

HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE is an FDA 510(k)-cleared medical device (K953491) 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.