# K131773: Brilliance Ict

- Pathway: 510(k) (Special)
- Applicant: Philips Healthcare (Cleveland)
- Decided: Sep 24, 2013 after 99 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K930090 (1993). 11 ancestors in all.
11 later devices descend from it; 1 cites it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060937: Brilliance Volume, Philips Medical Systems (Cleveland), Inc. (2006) Summary page 2.

## Most influential descendants
- K133674: Philips Iqon Spectral CT (2014), 10 descendants of its own
- K163711: IQon Spectral CT (2017), 7 descendants of its own
- K193454: IQon Spectral CT (2020), 6 descendants of its own
- K203020: Spectral CT (2021), 5 descendants of its own
- K240844: Spectral CT 7500 RT (2024), 3 descendants of its own

## Indications for use
The "Brilliance iCT" is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This device may include signal analysis and display equipment, patient and equipment supports, components, and accessories.

Source page: https://510kreport.com/device/K131773
Methodology: https://510kreport.com/methodology