Medical Device Manufacturer · US , Cavareno , TN

Cardioline S.P.A - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2015

Total

Cleared

Denied

Cardioline S.P.A has 4 FDA 510(k) cleared medical devices. Based in Cavareno, US.

Last cleared in 2023. Active since 2015. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Cardioline S.P.A Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Cardioline S.P.A

4 devices

1-4 of 4