K232698
- 510(k) number
- K232698
- Device name
- NemoScan
- Applicant
- Software Nemotec S.L. ES
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-01-18
- Date received
- 2023-09-05
- 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: K232698.pdf
Official FDA record: K232698
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.