Pressing DI Monticelli Rag. Stefano is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Pressing DI Monticelli Rag. Stefano - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Pressing DI Monticelli Rag. Stefano has 2 FDA 510(k) cleared medical devices. Based in Cattilica, IT.
Historical record: 2 cleared submissions from 1995 to 1998. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pressing DI Monticelli Rag. Stefano Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pressing DI Monticelli Rag. Stefano
2 devices