Assut Europe is one of 222 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
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.
510(k) submissions have been managed by Registrar Corp. as regulatory consultant.
FDA 510(k) Regulatory Record - Assut Europe
1 devices