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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