Cardio Tek, BV is one of 4769 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
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.
FDA 510(k) Regulatory Record - Cardio Tek, BV
2 devices