# K253103: Nexus DRF Digital X-ray Imaging System

- Pathway: 510(k) (Traditional)
- Applicant: Varex Imaging Corporation
- Decided: May 29, 2026 after 247 days
- Product code: JAA (System, X-Ray, Fluoroscopic, Image-Intensified)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K803130 (1981). 19 ancestors in all.
No later device cites it as a predicate yet.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130318: Nexus DRF Digital X-Ray Imaging System (with Paxscan 4343CB), Varian Medical Systems, X-Ray Products-Infimed (2013) Summary page 5.

## Indications for use
The Varex Nexus DRF Digital X-Ray Imaging System enables an operator to acquire, display, process, and export combined medical x-ray / fluoroscopy images for long-term storage. The Varex Nexus DRF Digital X-Ray Imaging System is intended for use in general radiographic examinations and applications (excluding mammography).

Source page: https://510kreport.com/device/K253103
Methodology: https://510kreport.com/methodology