Inogen - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Inogen has 1 FDA 510(k) cleared medical devices. Based in Goleta, US.
Last cleared in 2022. Active since 2022. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Inogen Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Inogen
1 devices