# K924459: Digiscan 2

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Dec 17, 1992 after 106 days
- Product code: IXK (System, Imaging, X-Ray, Electrostatic)
- Device class: 2
- Regulation: 21 CFR 892.1630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
194 later devices descend from it; 3 cite it directly.
0 of 195 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K983732: Thorax FD and Multix FD (1999), 187 descendants of its own
- K992794: Stingray DR, Model 1 (1999), 103 descendants of its own
- K013826: Axiom Aristos FX (Multi Purpose Radiography System) (2002), 81 descendants of its own
- K061054: Axiom Aristos FX Plus (2006), 80 descendants of its own
- K062623: Axiom Luminos DRF (2007), 78 descendants of its own

Source page: https://510kreport.com/device/K924459
Methodology: https://510kreport.com/methodology