Ev3 Neurovascular is one of 24544 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ev3 Neurovascular - FDA 510(k) Cleared Devices
Recent clearances: MERIDIAN GUIDEWIRE, HYPERGLIDE OCCLUSION BALLOON SYSTEM, HYPERFORM OCCLUSION BALLOON SYSTEM, MODEL 104-4112, 104-4113, 104-4127,104-4132,104, HYPERGLIDE OCCLUSION BALLOON SYSTEM, MODEL 104-4310, 104-4315
3
Total
3
Cleared
0
Denied
Ev3 Neurovascular has 3 FDA 510(k) cleared medical devices. Based in Lrvine, US.
Historical record: 3 cleared submissions from 2009 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ev3 Neurovascular Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ev3 Neurovascular
3 devices