Cardio Tek, BV is one of 18365 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardio Tek, BV - FDA 510(k) Cleared Devices
Recent clearances: EP-TRACER System, EP-TRACER SYSTEM, EP-TRACER SYSTEM, EP-TRACER SYSTEM
2
Total
2
Cleared
0
Denied
Cardio Tek, BV has 2 FDA 510(k) cleared medical devices. Based in Ballwin, US.
Historical record: 2 cleared submissions from 2014 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardio Tek, BV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Graematter, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cardio Tek, BV
2 devices