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 |
|---|---|---|---|
| K213730 | 11/26/2021 | MESI mTABLET TBI diagnostic system, MESI mTABLET TBI | Mesi, Development of Medical Devices, Ltd.; Mesi d.o.o. |
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