# K250181: AV Viewer

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems Nederland B.V.
- Decided: Jul 15, 2025 after 174 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: 9 generations back to K913770 (1991). 16 ancestors in all.
1 later device descends 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)
- K173588: Illumeo System, Philips Medical Systems Technologies, Ltd. (2018) Summary page 5.

## Most influential descendants
- K261465: Indira Cloud Viewer (2026), 0 descendants of its own

## Indications for use
The AV Viewer is an advanced visualization software intended to process and display images and associated data in a clinical setting. The software displays images of different modalities and timepoints, and performs digital image processing, measurements, manipulation, quantification and communication. The AV Viewer is not to be used for mammography.

Source page: https://510kreport.com/device/K250181
Methodology: https://510kreport.com/methodology