Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber

Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber is an FDA 510(k)-cleared medical device (K160109) 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 May 18, 2017. Regulation: 8.