Bose Corporation - FDA 510(k) Cleared Devices
2
Total
1
Cleared
1
Denied
Bose Corporation has 1 FDA 510(k) cleared medical devices. Based in Framingham, US.
Last cleared in 2021. Active since 2018. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Bose Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bose Corporation
2 devices