# K031198: SCANX 10

- Pathway: 510(k) (Traditional)
- Applicant: Air Techniques, Inc.
- Decided: Jun 20, 2003 after 65 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
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K101289: Scanx D5000 Series Scanner Model: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QB (2010), 0 descendants of its own
- K042397: SCANX 14 (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K031198
Methodology: https://510kreport.com/methodology