K252091
- 510(k) number
- K252091
- Device name
- Surgical Reality Viewer
- Applicant
- Medicalvr B.V. NL
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2026-01-29
- Date received
- 2025-07-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252091.pdf
Official FDA record: K252091
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.