510(k) K243459

Device
Ultimate rTMS for OCD (M-series)
Applicant
Brain Ultimate, Inc.
510(k) number
K243459
Product code
QCI
Decision
Substantially Equivalent (SESE)
Decision date
2025-04-17
Date received
2024-11-08
Regulation
882.5802
Classification name
Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Frank Ge
Address
5910 Shiloh Rd. E. Alpharetta GA US 30005 30005

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QCI#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K230657BTL-99-OCBTL Industries, Inc.2024-02-01
K233742CloudTMS Edge for OCDTeleemg, LLC2023-12-22
K231350OCD MT Cap (85-00397-000)Neuronetics2023-06-08
K221129CloudTMS for OCDTeleemg, LLC2023-03-10
K212289NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced Therapy System, NeuroStar TMS Therapy System, NeuroStar Advanced Therapy for Mental Health, NeuroStarNeuronetics, Inc.2022-05-06
K193006MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy systemTonica Elektronik A/S2020-08-09
K183303Brainsway Deep TMS SystemBrainsway , Ltd.2019-03-08
DEN170078Brainsway Deep Transcranial Magnetic Stimulation (DTMS) SystemBrainways , Ltd.2018-08-17