ResMed Corp - FDA 510(k) Cleared Devices

ResMed Corp has 18 FDA 510(k) cleared anesthesiology devices. Based in Poway, US.

Latest FDA clearance: Aug 2026. Active since 1997.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Resmed Pty , Ltd. as regulatory consultant.