Angiologica B. M. Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Angiologica B. M. Srl - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Angiologica B. M. Srl has 2 FDA 510(k) cleared medical devices. Based in San Martino Siccomario, Pavia, IT.
Historical record: 2 cleared submissions from 2005 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Angiologica B. M. Srl Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Angiologica B. M. Srl
2 devices