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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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