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Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K223670MESI mTablet ECG Diagnostic System, MESI mTablet ECGJuly 28, 2023
K213730MESI mTABLET TBI diagnostic system, MESI mTABLET TBIApril 21, 2022