Nucyro Vascular, LLC is one of 19585 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nucyro Vascular, LLC - FDA 510(k) Cleared Devices
Recent clearances: PolarCath Peripheral Dilatation System
1
Total
1
Cleared
0
Denied
Nucyro Vascular, LLC has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nucyro Vascular, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Nucyro Vascular, LLC
1 devices