Cardioline S.P.A is one of 16294 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, CARDIOLINE touchECG, ECG100+, ECG200+
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.
Regulatory submissions have been managed by Studio Tecnico Ing. Peluso and Studio Technico Ing. Peluso.
FDA 510(k) Regulatory Record - Cardioline S.P.A
4 devices