Angiologica B. M. Srl is one of 196 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
Recent clearances: HEMORPEX SYSTEM, REPOL ANGIMESH, ANGIMESH PRE, FOLDED MESH, REPOL PLUG BASIC, REPOL PLUG CAP, REPOL PLUG FLOWER AND WINGS MESH
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: General & Plastic Surgery.
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