K241390
- 510(k) number
- K241390
- Device name
- NeuroMatch
- Applicant
- LVIS Corporation CA · US
- Product code
- OMB — Automatic Event Detection Software For Full-Montage
- Decision date
- 2024-11-26
- Date received
- 2024-05-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K241390.pdf
Official FDA record: K241390
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.