# K022310: Advantage Windows X-Ray/MR Fusion

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, Inc.
- Decided: Aug 1, 2002 after 15 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: 2 generations back to K941223 (1994). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983256: Advantage Windows (AW) Fusion, GE Medical Systems (1998) Summary page 1.
- K010336: Advantage Windows CT/Pet Fusion, Ge Medical Systems, Inc. (2001)

## Most influential descendants
- K093234: Integrated Registration (2009), 0 descendants of its own

## Indications for use
Advantage Windows MR Fusion provides an easy means for comparison of three dimensional (3D) images from X-ray angiography (XR: providing anatomical imaging) and Magnetic Resonance (MR: providing anatomical imaging). It allows registration between two volumetric acquisitions, which may come from different acquisition modalities (X-Ray and MR), to help physicians in diagnostic radiology or therapy planning.

Source page: https://510kreport.com/device/K022310
Methodology: https://510kreport.com/methodology