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FDA 510(k) Applications Submitted by NeuroOne Medical Technologies Corp.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K222404
08/09/2022
Evo« sEEG System
NeuroOne Medical Technologies Corp.
K211367
05/04/2021
Evo sEEG System
NeuroOne Medical Technologies Corp.
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