# K003628: Magnetom Rhapsody System

- Pathway: 510(k) (Abbreviated)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Jan 23, 2001 after 60 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K020573: Modification to Magnetom Rhapsody System (2002), 0 descendants of its own

## Recalls of this device
- Feb 28, 2003 · Not classified · Z-1087-03: software problem This error may cause the loss of peripheral image information when there is a difference between the dimensions of the image matrix and the display segment.

Source page: https://510kreport.com/device/K003628
Methodology: https://510kreport.com/methodology