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MESI mTablet ECG Diagnostic System, MESI mTablet ECG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223670
510(k) Type
Traditional
Applicant
MESI, Development of Medical Devices, Ltd; MESI, D.O.O.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
7/28/2023
Days to Decision
233 days
Submission Type
Summary

MESI mTablet ECG Diagnostic System, MESI mTablet ECG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223670
510(k) Type
Traditional
Applicant
MESI, Development of Medical Devices, Ltd; MESI, D.O.O.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
7/28/2023
Days to Decision
233 days
Submission Type
Summary