# K162025: IntelliSpace Portal Platform

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems Nederlands B.V.
- Decided: Oct 18, 2016 after 88 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: 5 generations back to K945188 (1995). 17 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081985: AW Server, Ge Medical Systems, LLC (2008) Summary page 4.

## Most influential descendants
- K200899: Quantib AI Node (2020), 0 descendants of its own

## Indications for use
Philips IntelliSpace Portal Platform is a software medical device that allows multiple users to remotely access clinical applications from compatible computers on a network. The system allows networking, selection, processing and filming of multimodality DICOM images. This software is for use with off-the-shelf PC computer technology that meets defined minimum specifications . Philips IntelliSpace Portal Platform is intended to be used by trained professionals, including but not limited to physicians and medical technicians. This medical device is not to be used for mammography. The device is not intended for diagnosis of lossy compressed images.

Source page: https://510kreport.com/device/K162025
Methodology: https://510kreport.com/methodology