K250239
- 510(k) number
- K250239
- Device name
- NeuroMatch
- Applicant
- LVIS Corporation CA · US
- Product code
- OLX — Source Localization Software For Electroencephalogra
- Decision date
- 2025-05-23
- Date received
- 2025-01-27
- 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: K250239.pdf
Official FDA record: K250239
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.