K261228
- 510(k) number
- K261228
- Device name
- QuickVision Ultimate rTMS
- Applicant
- Brain Ultimate, Inc. GA · US
- Product code
- OBP — Transcranial Magnetic Stimulator
- Decision date
- 2026-08-14
- Date received
- 2026-04-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K261228.pdf
Official FDA record: K261228
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.