Elective Vascular Intervention Inc. (Evi) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Elective Vascular Intervention Inc. (Evi) - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Elective Vascular Intervention Inc. (Evi) has 1 FDA 510(k) cleared medical devices. Based in Walnut Creek, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Elective Vascular Intervention Inc. (Evi) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Elective Vascular Intervention Inc. (Evi)
1 devices