# K132934: Multix Select DR

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medi Cal Solutions, Inc.
- Decided: Apr 10, 2014 after 204 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K801623 (1980). 65 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 69 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121513: Multix Fusion, Siemens Medical Solution (2012) Summary page 3.

## Most influential descendants
- K181413: uDR 592h, uDR 596i (2018), 2 descendants of its own
- K192293: uDR 592h, uDR 596i (2019), 1 descendant of its own
- K252000: uDR Arria & uDR Aris (2025), 0 descendants of its own

## Indications for use
The Multix Select DR is a digital system used for making X-ray exposures of the head, spinal column, abdomen, thorax (lungs), internal organs and extremities with/without using conventional film/screen and CR-systems, and may be used on pediatric, adult and bariatric patients. The Multix Select DR system is not meant for mammography.

Source page: https://510kreport.com/device/K132934
Methodology: https://510kreport.com/methodology