Eurospital S.P.A. is one of 13017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eurospital S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: Calprest, EasyCal, CalprestNG, EasyCal, Calprest NG
4
Total
4
Cleared
0
Denied
Eurospital S.P.A. has 4 FDA 510(k) cleared medical devices. Based in Woodstock, US.
Historical record: 4 cleared submissions from 2014 to 2019. 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.
510(k) submissions have been managed by Catherine L. Wong as regulatory consultant.
FDA 510(k) Regulatory Record - Eurospital S.P.A.
4 devices