# K082336: XR-Express

- Pathway: 510(k) (Traditional)
- Applicant: New Mexico Software, Inc.
- Decided: Oct 15, 2008 after 62 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
Longest line of descent: 5 generations back to K945188 (1995). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063221: Medweb Advanced 3D Web Pacs, Nexsys Electronics, Inc. (2006) Summary page 2.

## Indications for use
XR-EXpress is a PACS and teleradiology system used to receive DICOM images, scheduling information and textual reports, organize and store them in an internal format, and to make that information available across a network via web and customized user interfaces. XR-EXpress is for hospitals, imaging centers, nursing homes, radiologist reading practices, and any user who requires and is granted access to patient image, demographic, and report information. Lossy compressed mammographic images and digitized film screen images must not be reviewed for primary image interpretations. Mammographic images may only be interpreted using an FDA approved monitor that offers at least 5 Mpixel resolution and meets other technical specifications reviewed and accepted by FDA.

Source page: https://510kreport.com/device/K082336
Methodology: https://510kreport.com/methodology