Medical Device Manufacturer · US , Woodstock , GA

Eurospital S.P.A. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014
4
Total
4
Cleared
0
Denied

Eurospital S.P.A. has 4 FDA 510(k) cleared medical devices. Based in Woodstock, US.

Last cleared in 2019. Active since 2014. Primary specialty: Immunology.

Browse the FDA 510(k) cleared devices submitted by Eurospital S.P.A. Filter by specialty or product code using the sidebar.

4 devices
1–4 of 4
Filters
Filter by Specialty
All4 Immunology 4