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CARDIOLINE touchECG

Page Type
Cleared 510(K)
510(k) Number
K160746
510(k) Type
Traditional
Applicant
CARDIOLINE S.p.A
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
11/2/2016
Days to Decision
229 days
Submission Type
Summary

CARDIOLINE touchECG

Page Type
Cleared 510(K)
510(k) Number
K160746
510(k) Type
Traditional
Applicant
CARDIOLINE S.p.A
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
11/2/2016
Days to Decision
229 days
Submission Type
Summary