Neurosoft , Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Neurosoft , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Abano Terme, Padova, IT.
Last cleared in 2022. Active since 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neurosoft , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Makromed, Inc. and Corticare, Inc..
3 devices