Avia Vascular is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avia Vascular - FDA 510(k) Cleared Devices
Recent clearances: 20G Open-System Ally Device Kit (AV100000), 22G Open-System Ally Device Kit (AV110000)
1
Total
1
Cleared
0
Denied
Avia Vascular has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Avia Vascular Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medventure Health as regulatory consultant.
FDA 510(k) Regulatory Record - Avia Vascular
1 devices