Brainsway Deep Transcranial Magnetic Stimulation (DTMS) System— 510(k) DEN170078

Name: FDA 510(k) clearance DEN170078
Creator: U.S. Food and Drug Administration
Published: 2018-08-17

Unknown

Brainways , Ltd.

FDA 510(k) clearance DEN170078 for Brainsway Deep Transcranial Magnetic Stimulation (DTMS) System, Unknown on 2018-08-17. Applicant: Brainways , Ltd.. Device class: 2.

Clearance details

Applicant: Brainways , Ltd.
Product code: Code QCI
Device class: Class 2
Regulation: 21 CFR 882.5802
Advisory panel: Neurology
Date received: 2017-09-29
Decision date: 2018-08-17
Decision: Unknown
Clearance type: Direct
Location: Har Hotzvim, IL

View on FDA.gov ↗

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