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

FDA Regulatory Profile

Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd. 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 December 11, 2020.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K201046Automated ankle brachial pressure index measuring device, MESI mTABLET systemDecember 11, 2020
K172655Automated ankle brachial pressure index measuring deviceJanuary 11, 2018

FDA data resources