Truerelief - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Truerelief has 1 FDA 510(k) cleared medical devices. Based in Santa Monica, US.
Last cleared in 2021. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Truerelief Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Allenbridge Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Truerelief
1 devices