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.
510(k) submissions have been managed by Pathmaker FDA Law, PLLC as regulatory consultant.
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