Ensite Vacular, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ensite Vacular, LLC - FDA 510(k) Cleared Devices
Recent clearances: SiteSeal Femoral Compression Device
1
Total
1
Cleared
0
Denied
Ensite Vacular, LLC has 1 FDA 510(k) cleared medical devices. Based in Olathe, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ensite Vacular, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by TAMM Net, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ensite Vacular, LLC
1 devices