# K913525: Mobile X-Ray System

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Oct 23, 1991 after 76 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.
24 later devices descend from it; 1 cites it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Siremobil 3 mobile x-ray system: named in the summary without a submission number

## Most influential descendants
- K963093: Siremobil Compact (1996), 23 descendants of its own
- K040066: Siremobile C06 (2004), 21 descendants of its own
- K051133: Arcadis Avantic (2005), 20 descendants of its own
- K132094: Cios Alpha (2014), 19 descendants of its own
- K153244: Cios Fusion (2016), 15 descendants of its own

## Indications for use
X-ray imaging for surgery, traumatology, orthopedics, endoscopy, intensive care, and interventional vascular procedures.

Source page: https://510kreport.com/device/K913525
Methodology: https://510kreport.com/methodology