TURBO AIR COMPRESSOR 8000

TURBO AIR COMPRESSOR 8000 is an FDA 510(k)-cleared medical device (K883829) manufactured by Necon Medical, 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 March 22, 1989. Regulation: 8.