# K123005: Ddrversa Motion

- Pathway: 510(k) (Special)
- Applicant: Swissray Medical AG
- Decided: Dec 7, 2012 after 71 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- 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: 5 generations back to K001201 (2000). 6 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110828: Ddrelement, Swissray Medical AG (2011) Summary page 1.
- K083109: Suinsa Diagnostic X-Ray System, Suinsa (2008) Summary page 1.

## Most influential descendants
- K141381: Duradiagnost (2014), 3 descendants of its own
- K163410: DigitalDiagnost C50 (2017), 1 descendant of its own
- K201725: DigitalDiagnost C50 (2020), 0 descendants of its own
- K201640: DuraDiagnost (2020), 0 descendants of its own

## Indications for use
The ddRVersaTrM Motion System is intended for use by a qualified/trained doctor or technician on subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position. (Not for mammography)

Source page: https://510kreport.com/device/K123005
Methodology: https://510kreport.com/methodology