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

Brainsway Deep (DTMS) System

K Number: K203616 · Decision Apr 16, 2021
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
1
Applicant Total
11
Review Days
127

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Brainsway Deep (DTMS) System
K Number
K203616
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5802
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Brainsway , Ltd.
Date Received
December 10, 2020
Decision Date
April 16, 2021
Product Code
QMD
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
QMD Transcranial Magnetic Stimulation System For Smoking Cessation

Similar 510(k) Clearances

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

View all

Other Clearances by Brainsway , Ltd.

K Number Device Name
K251391 BrainsWay Deep TMS System
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
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. →