# K102344: Mdixon Software Option for Intera 1.5T, Achieva 1.5T & Achieva 3.0T MR Systems

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems Nederland B.V.
- Decided: Nov 9, 2010 after 83 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
Longest line of descent: 6 generations back to K962061 (1996). 19 ancestors in all.
1 later device descends from it; 1 cites it directly.
8 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063559: Achieva, Intera and Panorama 1.0T, Release 2.5, Philips Medical Systems (2007) Summary page 1.
- K072998: Ideal Software Option for GE MR Scanners, Ge Medical Systems, LLC (2007) Summary page 1.

## Most influential descendants
- K143128: mDIXON XD (2015), 0 descendants of its own

## Indications for use
mDIXON is a software option intended for use on Intera 1.5T, Achieva 1.5T and Achieva 3T MR Systems. It's indicated for magnetic resonance imaging of the chest, abdomen and pelvis. mDIXON is a multipoint(echo) method for 3D clinical imaging with the possibility to reformat into multiple planes (axial, sagittal and coronal). mDixon provides improved fat suppression, increased scan speed in addition and/or an improved signal-to-noise.

Source page: https://510kreport.com/device/K102344
Methodology: https://510kreport.com/methodology