K233391
- 510(k) number
- K233391
- Device name
- cCeLL - In vivo
- Applicant
- VPIX Medical, Inc. KR
- Product code
- GWG — Endoscope, Neurological
- Decision date
- 2024-08-21
- Date received
- 2023-10-02
- 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: K233391.pdf
Official FDA record: K233391
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.