# K090655: Portable X-Ray System, Model Powermax 1260

- Pathway: 510(k) (Traditional)
- Applicant: Source-Ray, Inc.
- Decided: Jul 14, 2009 after 125 days
- Product code: IZL (System, X-Ray, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K163063: UC-5000 Mobile X-Ray (2016), 0 descendants of its own

## Indications for use
The Model PowerMax 1260 Portable X-Ray System is intended for General Purpose Portable Radiographic Applications

Source page: https://510kreport.com/device/K090655
Methodology: https://510kreport.com/methodology