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Cardioline S.P.A

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220526HD+12, HD+15May 15, 2023
K160746CARDIOLINE touchECGNovember 2, 2016
K160840ECG100+, ECG200+August 12, 2016
K150289CARDIOLINE HD+August 27, 2015