Resmed, Ltd. - FDA 510(k) Cleared Devices

Resmed, Ltd. has 103 FDA 510(k) cleared anesthesiology devices. Based in Poway, US.

Historical record: 103 cleared submissions from 1996 to 2019.

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

Regulatory submissions have been managed by Resmed Corp (Registration Number: 3007573469) and Resmed Corp. 2 devices have linked clinical trials registered on ClinicalTrials.gov.