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

FDA Regulatory Profile

Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 28, 2023.

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

FDA data resources