K232159
- 510(k) number
- K232159
- Device name
- QEVO System
- Applicant
- Carl Zeiss Meditec, AG DE
- Product code
- GWG — Endoscope, Neurological
- Decision date
- 2023-09-21
- Date received
- 2023-07-20
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K232159.pdf
Official FDA record: K232159
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.