# K173588: Illumeo System

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems Technologies, Ltd.
- Decided: Jan 12, 2018 after 53 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K913770 (1991). 15 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160315: I4 (Integrated Intelligent Imaging Informatics) system, Philips Medical Systems Nederland B.V. (2016) Summary page 5.

## Most influential descendants
- K250181: AV Viewer (2025), 1 descendant of its own
- K261465: Indira Cloud Viewer (2026), 0 descendants of its own

## Indications for use
Illumeo system is an image management system intended to be used by trained professionals, including but not limited to radiologists. Illumeo system is a software package used with general purpose computing hardware to acquire, store, distribute, process and display images and associated data throughout a clinical environment. The software performs digital image processing, measurement, manipulation and quantification of images, communication and storage. This device is not to be used for mammography.

Source page: https://510kreport.com/device/K173588
Methodology: https://510kreport.com/methodology