# K992103: C-Quest

- Pathway: 510(k) (Traditional)
- Applicant: Wuestec Medical, Inc.
- Decided: Sep 1, 1999 after 71 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K070123: TCA 5R / 5S (2007), 0 descendants of its own

## Indications for use
The 4R and 5 mobile x-ray unit with image intensifier system has been designed for diagnosis, suitable for x-ray examinations, and in particular for radioscopy, and radiography dedicated to: o 7 Traumatology o Paediatrics . Interventional radiology o Peace maker implantation . Operating theater . Intensive care ) Respiratory system o Skeleton This device does not foresee any interaction with medicine, while the possibility of an interface with some devices like VCR or THERMAL PRINTER is foreseen.

Source page: https://510kreport.com/device/K992103
Methodology: https://510kreport.com/methodology