K253103
- 510(k) number
- K253103
- Device name
- Nexus DRF Digital X-ray Imaging System
- Applicant
- Varex Imaging Corporation UT · US
- Product code
- JAA — System, X-Ray, Fluoroscopic, Image-Intensified
- Decision date
- 2026-05-29
- Date received
- 2025-09-24
- 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: K253103.pdf
Official FDA record: K253103
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.