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CARDIOLINE touchECG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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