EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.

EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR. is an FDA 510(k)-cleared medical device (K800456) manufactured by Khi, 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 17, 1980. Regulation: 8.