Last synced on 14 November 2025 at 11:06 pm

MESI mTablet ECG Diagnostic System, MESI mTablet ECG

Page Type
Cleared 510(K)
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)
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