# K151924: Q-Rad Radiographic System with Auto-Tracker Option

- Pathway: 510(k) (Special)
- Applicant: Quantum Medical Imaging Divison of Carestream
- Decided: Aug 7, 2015 after 25 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
Longest line of descent: 1 generation back to K011486 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011486: Q-Rad Radiographic System, Quantum Medical Imaging, LLC (2001) Summary page 4.

## Indications for use
The Q-Rad Radiographic System is indicated for use in obtaining diagnostic quality radiographic images to aid the physician with diagnosis. The system can be used to perform radiographic imaging of various portions of the human body, including the skull, spinal column, extremities, chest, abdomen and other body parts. The Q-Rad System is not indicated for use in mammography.

Source page: https://510kreport.com/device/K151924
Methodology: https://510kreport.com/methodology