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FDA 510(k) Applications Submitted by BrainsWay Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K210201
01/25/2021
Deep Transcranial Magnetic Stimulation (DTMS) System
Brainsway Ltd.
K220819
03/21/2022
BrainsWay Deep TMS System
BrainsWay Ltd.
K200957
04/09/2020
Brainsway Deep TMS System
Brainsway Ltd.
K173540
11/15/2017
Brainsway Deep (DTMS) System
Brainsway Ltd.
K203616
12/10/2020
Brainsway Deep (DTMS) System
Brainsway Ltd.
K203735
12/21/2020
Brainsway Deep TMS System
Brainsway Ltd.
K183303
11/27/2018
Brainsway Deep TMS System
Brainsway Ltd.
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