K233908
- 510(k) number
- K233908
- Device name
- cNeuro cDAT
- Applicant
- Combinostics OY FI
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-07-01
- Date received
- 2023-12-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233908.pdf
Official FDA record: K233908
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.