K240575
- 510(k) number
- K240575
- Device name
- WaveGuard Net EEG Cap (NA-245, NA-255, NA-261, NA-265, NA-271, NA-281)
- Applicant
- Eemagine Medical Imaging Solutions GmbH DE
- Product code
- GXY — Electrode, Cutaneous
- Decision date
- 2024-11-25
- Date received
- 2024-03-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K240575.pdf
Official FDA record: K240575
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.