FDA 510(k) Applications Submitted by Cardioline S.P.A

FDA 510(k) Number Submission Date Device Name Applicant
K220526 02/24/2022 HD+12, HD+15 Cardioline S.P.A
K150289 02/05/2015 CARDIOLINE HD+ CARDIOLINE S.p.A
K160746 03/18/2016 CARDIOLINE touchECG CARDIOLINE S.p.A
K160840 03/28/2016 ECG100+, ECG200+ CARDIOLINE S.p.A


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