Mivi Neurovascular is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mivi Neurovascular - FDA 510(k) Cleared Devices
Recent clearances: Q3 Distal Access Catheter, Q4 Distal Access Catheter, Q5 Distal Access Catheter, Q6Distal Access Catheter
1
Total
1
Cleared
0
Denied
Mivi Neurovascular has 1 FDA 510(k) cleared medical devices. Based in Eden Prarie, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Mivi Neurovascular Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mivi Neurovascular
1 devices