# K003266: Siremobil Iso-C 3D

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Dec 1, 2000 after 44 days
- Product code: OXO (Image-Intensified Fluoroscopic X-Ray System, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
440 later devices descend from it; 7 cite it directly.
2 of 441 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
- K011447: IN Space 3D (2001), 244 descendants of its own
- K043469: Syngo Inspace 4D (2005), 218 descendants of its own
- K071513: Inspace 4D Software Package with Extended Functionality (2007), 210 descendants of its own
- K062673: Modification to Syngo Inspace 4D (2006), 172 descendants of its own
- K062351: Syngo Dual Energy (2006), 169 descendants of its own

Source page: https://510kreport.com/device/K003266
Methodology: https://510kreport.com/methodology