Neuro20 Technologies - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Neuro20 Technologies has 1 FDA 510(k) cleared medical devices. Based in Tampa, US.
Last cleared in 2023. Active since 2023. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Neuro20 Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Neuro20 Technologies
1 devices