# K082064: Radvision ET Diagnostic X-Ray System

- Pathway: 510(k) (Special)
- Applicant: Almana Medical Imaging
- Decided: Aug 22, 2008 after 32 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: 3 generations back to K001201 (2000). 3 ancestors in all.
6 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072659: Rad Vision, Models E and EU, Almana Medical Imaging (2007) Summary page 1.

## Most influential descendants
- K083109: Suinsa Diagnostic X-Ray System (2008), 5 descendants of its own
- K123005: Ddrversa Motion (2012), 4 descendants of its own
- 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

## Indications for use
This Radiographic System is intended for use by a qualified/trained doctor or technician on both adult and pediatric 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.

Source page: https://510kreport.com/device/K082064
Methodology: https://510kreport.com/methodology