SIMEOX 200 Airway Clearance Device

SIMEOX 200 Airway Clearance Device is an FDA 510(k)-cleared medical device (K241091) manufactured by Inogen, 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 22, 2024. Regulation: 8.