Tursiop Technologies, LLC is one of 20523 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tursiop Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: CAROTID COIL GE 1.5T, TT1 GENERAL PURPOSE COIL
2
Total
2
Cleared
0
Denied
Tursiop Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Historical record: 2 cleared submissions from 2008 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Tursiop Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Tursiop Technologies, LLC
2 devices