FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

BrainsWay Deep TMS System

K Number: K251391 · Decision Nov 7, 2025
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
65
Applicant Total
11
Review Days
186

Basic Information

Device Name
BrainsWay Deep TMS System
K Number
K251391
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5805
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Brainsway , Ltd.
Date Received
May 5, 2025
Decision Date
November 7, 2025
Product Code
OBP
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OBP Transcranial Magnetic Stimulator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OBP), ordered by most recent decision date.

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Other Clearances by Brainsway , Ltd.

K Number Device Name
K251449 BrainsWay Deep TMS System
K222196 Deep TMS System
K220819 BrainsWay Deep TMS System
K210201 Deep Transcranial Magnetic Stimulation (DTMS) System
K203735 Brainsway Deep TMS System
K203616 Brainsway Deep (DTMS) System
K200957 Brainsway Deep TMS System
K183303 Brainsway Deep TMS System
K173540 Brainsway Deep (DTMS) System
K122288 BRAINSWAY DEEP TMS SYSTEM
Search all 11 clearances from Brainsway , Ltd. →