Tatara Vascular, LLC is one of 18410 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tatara Vascular, LLC - FDA 510(k) Cleared Devices
Recent clearances: PW Guidewires
1
Total
1
Cleared
0
Denied
Tatara Vascular, LLC has 1 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tatara Vascular, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jmcs, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Tatara Vascular, LLC
1 devices