Assut Europe is one of 112 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Assut Europe - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Assut Europe has 1 FDA 510(k) cleared medical devices. Based in Magliano Dei Marsi, IT.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Assut Europe Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Assut Europe
1 devices