Brainsway Deep TMS System
K-Number: K200957 · 2020-08-21
ApplicantBrainsway , Ltd.
Decision Date2020-08-21
Product CodeQMD
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Brainsway Deep TMS System is a medical device manufactured by Brainsway , Ltd.. It received FDA 510(k) clearance on 2020-08-21 under approval number K200957. The device is classified under product code QMD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Brainsway Deep TMS System?
Brainsway Deep TMS System is a medical device that received FDA 510(k) clearance on 2020-08-21. It is manufactured by Brainsway , Ltd.. The 510(k) number is K200957.
When was Brainsway Deep TMS System approved by the FDA?
Brainsway Deep TMS System received FDA 510(k) clearance on 2020-08-21, under approval number K200957.
What company makes Brainsway Deep TMS System?
Brainsway Deep TMS System is manufactured by Brainsway , Ltd..
What is the FDA product code for Brainsway Deep TMS System?
The FDA product code for Brainsway Deep TMS System is QMD.
Other Devices by Brainsway , Ltd.
Related Devices (Code: QMD)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.