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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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