# K070563: Vidar Vision 2000

- Pathway: 510(k) (Traditional)
- Applicant: Vidar Systems Corp.
- Decided: Mar 16, 2007 after 17 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: 1 generation back to K974863 (1998). 1 ancestor in all.
5 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K974863: Imix Digital Thorax System, Advanced Instrument Development, Inc. (1998) Summary page 2.

## Most influential descendants
- K071193: Vidar Vision 3000 and 4000 X-Ray Systems (2007), 4 descendants of its own
- K073114: Imix Insight X-Ray Systems (2008), 2 descendants of its own
- K101435: Imix Panorad and Somarad (2010), 1 descendant of its own
- K113855: Panorad, Panorad SL (2012), 0 descendants of its own
- K082261: Dxrad Models DX800 or DX808 Digital Diagnostic Radiographic Systems (2008), 0 descendants of its own

## Indications for use
The VIDAR Vision 2000 is indicated for use in generating radiographic images of human anatomy. It is a Solid State X-ray Imaging system intended to replace radiographic film/screen systems in all general-purpose diagnostic procedures. The VIDAR Vision 2000 is not indicated for diagnostic X-ray mammography.

Source page: https://510kreport.com/device/K070563
Methodology: https://510kreport.com/methodology