LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber is an FDA 510(k)-cleared medical device (K210558) manufactured by Thayer Medical Corporation. 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 31, 2022. Regulation: 8.