# K910902: VMX Mobile X-Ray System

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Sep 9, 1991 after 188 days
- Product code: IZL (System, X-Ray, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1720
- 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.
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. FDA has not posted a summary or statement for it, so its predicates are not known.

## 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

## Recalls of this device
- Jan 23, 2012 · Class II · Z-1083-2013: GE Healthcare has become aware of an issue associated with the base casting for the articulated arm of your VMX and VMX Plus Mobile X-ray systems that may impact Operator or Patient safety.

Source page: https://510kreport.com/device/K910902
Methodology: https://510kreport.com/methodology