# K974863: Imix Digital Thorax System

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Instrument Development, Inc.
- Decided: Mar 17, 1998 after 78 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
No predicates in its family tree.
8 later devices descend from it; 3 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K070563: Vidar Vision 2000 (2007), 5 descendants of its own
- 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
- K992955: Xplorer 1000 (2000), 1 descendant of its own

## Indications for use
General Radiography as prescribed by competent authority.

Source page: https://510kreport.com/device/K974863
Methodology: https://510kreport.com/methodology