K260402
- 510(k) number
- K260402
- Device name
- MeRT System
- Applicant
- Wave Neuroscience CA · US
- Product code
- SIG — Transcranial Magnetic Stimulation System For Post Tr
- Decision date
- 2026-06-03
- Date received
- 2026-02-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K260402.pdf
Official FDA record: K260402
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.