# K974134: X-Sight Digital Imaging System

- Pathway: 510(k) (Traditional)
- Applicant: Stallion Technologies, Inc.
- Decided: Jan 27, 1998 after 85 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The X-Sight device is indicated for reading, storing, and converting image data from fluoroscopic x-ray systems.

Source page: https://510kreport.com/device/K974134
Methodology: https://510kreport.com/methodology