RES Q AIR SYSTEM MODEL HT-1000

RES Q AIR SYSTEM MODEL HT-1000 is an FDA 510(k)-cleared medical device (K926161) manufactured by C.F. Electronics, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 25, 1993. Regulation: 8.