K232779
- 510(k) number
- K232779
- Device name
- QUEX ED; QUEX S
- Applicant
- Qx World, Ltd. HU
- Product code
- OMC — Reduced- Montage Standard Electroencephalograph
- Decision date
- 2024-10-11
- Date received
- 2023-09-11
- 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: K232779.pdf
Official FDA record: K232779
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.