FDA 510(k) Applications Submitted by MESI, Development of Medical Devices, Ltd; MESI, D.O.O.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K223670 | 12/07/2022 | MESI mTablet ECG Diagnostic System, MESI mTablet ECG | MESI, Development of Medical Devices, Ltd; MESI, D.O.O. |
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