MAXI-MISER HUMIDIFIER INSERT 1030

MAXI-MISER HUMIDIFIER INSERT 1030 is an FDA 510(k)-cleared medical device (K842795) manufactured by Nova-Ventrx. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 1984. Regulation: 8.