# K180925: uMR 570

- Pathway: 510(k) (Traditional)
- Applicant: Shanghai United Imaging Healthcare Co., Ltd.
- Decided: Jun 6, 2018 after 58 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: 11 generations back to K971684 (1997). 33 ancestors in all.
7 later devices descend from it; 1 cites it directly.
3 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132951: Magnetom Aera, Siemens Medical Solutions USA, Inc. (2013) Summary page 5.

## Most influential descendants
- K200024: uMR 570 (2020), 6 descendants of its own
- K201540: uMR570 (2020), 5 descendants of its own
- K222755: uMR 680 (2023), 3 descendants of its own
- K240744: uMR 680 (2024), 2 descendants of its own
- K243397: uMR 680 (2025), 1 descendant of its own

## Indications for use
The uMR 570 system is indicated for use as a magnetic resonance diagnostic device (MRDD) that produces sagittal, transverse, coronal, and oblique cross sectional images, and spectroscopic images, and that display internal anatomical structure and/or function of the head, body and extremities. These images and the physical parameters derived from the images when interpreted by a trained physician yield information that may assist the diagnosis. Contrast agents may be used depending on the region of interest of the scan.

Source page: https://510kreport.com/device/K180925
Methodology: https://510kreport.com/methodology