HEATER, IMMERSION W/ HUMIDIFIER & NEBUL.

HEATER, IMMERSION W/ HUMIDIFIER & NEBUL. is an FDA 510(k)-cleared medical device (K760037) manufactured by Inspiron Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 15, 1976. Regulation: 8.