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ECG100+, ECG200+

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160840
510(k) Type
Traditional
Applicant
Cardioline S.P.A
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
8/12/2016
Days to Decision
137 days
Submission Type
Summary

ECG100+, ECG200+

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160840
510(k) Type
Traditional
Applicant
Cardioline S.P.A
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
8/12/2016
Days to Decision
137 days
Submission Type
Summary