K230125
- 510(k) number
- K230125
- Device name
- Neuroblade System
- Applicant
- Clearmind Biomedical TW
- Product code
- GWG — Endoscope, Neurological
- Decision date
- 2023-10-13
- Date received
- 2023-01-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K230125.pdf
Official FDA record: K230125
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.