# K803130: Multix U. Bucky Table X-Ray Unit

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Corp.
- Decided: Jan 28, 1981 after 47 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
198 later devices descend from it; 1 cites it directly.
0 of 199 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
- K971452: Multix Top/Pro Radiographic X-Ray Table (1997), 197 descendants of its own
- 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

## Recalls of this device
- Apr 15, 2003 · Not classified · Z-0987-03: the back up safety catch may not function properly

Source page: https://510kreport.com/device/K803130
Methodology: https://510kreport.com/methodology