# K011486: Q-Rad Radiographic System

- Pathway: 510(k) (Traditional)
- Applicant: Quantum Medical Imaging, LLC
- Decided: Jun 20, 2001 after 36 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.
11 later devices descend from it; 5 cite it directly.
0 of 12 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
- K072010: Quantum Direx System (2007), 5 descendants of its own
- K080905: Quantum/ Canon Cxdi Integration System, Model QG-Dig-Cxdi (2008), 4 descendants of its own
- K193574: Q-Rad System (2020), 3 descendants of its own
- K201373: DRX-Compass (2020), 2 descendants of its own
- K073632: Intuition, Model 0170 (2008), 2 descendants of its own

Source page: https://510kreport.com/device/K011486
Methodology: https://510kreport.com/methodology