Ims Giotto S.P.A. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ims Giotto S.P.A. has 2 FDA 510(k) cleared medical devices. Based in Sasso Marconi, IT.
Last cleared in 2021. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ims Giotto S.P.A. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by THEMA S.r.l. as regulatory consultant.
2 devices