AireHealth NebulizerTM

AireHealth NebulizerTM is an FDA 510(k)-cleared medical device (K201167) manufactured by Airehealth, 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 December 2, 2020. Regulation: 8.