Micromed S.P.A. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Micromed S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: LED PHOTIC System, SD LTM STIM Cortical Stimulator, Micromed BRAIN QUICK system
4
Total
4
Cleared
0
Denied
Micromed S.P.A. has 4 FDA 510(k) cleared medical devices. Based in Mogliano Veneto (Tv), IT.
Last cleared in 2021. Active since 2008. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Micromed S.P.A. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Eas Consulting Group and Spectramedex, LLC.
FDA 510(k) Regulatory Record - Micromed S.P.A.
4 devices