# K003899: Ifis-SA Integrated Fuctional Imaging System

- Pathway: 510(k) (Traditional)
- Applicant: Mri Devices Corp.
- Decided: Mar 15, 2001 after 87 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023130: Eloquence, Integrated Functional Imaging System (2002), 7 descendants of its own
- K052467: Brain Viewrx Viewer, Version 1.0 (2005), 5 descendants of its own
- K063031: Prism View, Model (2006), 2 descendants of its own
- K061255: Brainacquirerx / Brainprocessrx Data Suite Version 1.0 (2006), 2 descendants of its own
- K082964: Prism Acquire (Version 1.5), Prism Process (Version 1.5), Prism View (Version 2.5) (2009), 1 descendant of its own

Source page: https://510kreport.com/device/K003899
Methodology: https://510kreport.com/methodology