Thayer Medical Corporation - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Thayer Medical Corporation has 4 FDA 510(k) cleared medical devices. Based in Tucson, US.
Latest FDA clearance: Jun 2024. Active since 2011. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Thayer Medical Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Thayer Medical Corporation
4 devices
Cleared
Jun 18, 2024
MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter
Anesthesiology
225d
Cleared
Apr 01, 2022
LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber
Anesthesiology
400d
Cleared
May 19, 2017
Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber
Anesthesiology
486d
Cleared
Sep 29, 2011
MINISPACER(R) MDI ADAPTER WITH COUNTER INCREMENTING ACTUATOR
Anesthesiology
115d