Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber

K160109 is the FDA 510(k) clearance record for Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber, a class II device, cleared for Thayer Medical Corporation on 2017-05-19 under FDA product code NVP (Holding Chambers, Direct Patient Interface). FDA's definition for product code NVP reads: "Holding chambers are devices that are used with nebulizers and metered dose inhalers and are comprised of a reservoir into which an aerosol medication is dispensed. A holding chamber uses a valved mouthpiece through which the patient...". FDA records list 19 510(k) clearances for THAYER MEDICAL CORPORTATION, from 1988-07-18 to 2024-06-18. As of 2026-09-10, FDA records show no recalls naming K160109.