# K001201: Multix Compact K and Multix L Radiographic X-Ray Systems

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Jun 1, 2000 after 49 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.
164 later devices descend from it; 3 cite it directly.
0 of 165 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
- K012546: Optima Urs Universal Radiographic System (2001), 158 descendants of its own
- K042876: Urs LP Digital, Millennium, Radpro (2004), 138 descendants of its own
- K062335: Sedecal X Plus LP Plus (2006), 99 descendants of its own
- K090238: Sedecal X-Plus LP Plus Digital Diagnostic X-Ray Systems (2009), 46 descendants of its own
- K082604: Viztek DR, Models: DR1000, DR3000, DR4000 (2008), 41 descendants of its own

Source page: https://510kreport.com/device/K001201
Methodology: https://510kreport.com/methodology