Class Class II

BrainsWay Deep TMS System (K251391)

K251391 2025-11-07 Traditional
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Description

BrainsWay Deep TMS System by Brainsway , Ltd., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251391
Clearance Date2025-11-07
Clearance TypeTraditional
Product CodeOBP
Regulation Number882.5805

Categories

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