Cardioline S.P.A is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardioline S.P.A - FDA 510(k) Cleared Devices
Recent clearances: HD+12, HD+15
4
Total
4
Cleared
0
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) Regulatory Record - Cardioline S.P.A
4 devices