# K233673: uMR Jupiter

- Pathway: 510(k) (Traditional)
- Applicant: Shanghai United Imaging Healthcare Co., Ltd.
- Decided: Apr 26, 2024 after 162 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: 17 generations back to K971684 (1997). 41 ancestors in all.
1 later device descends from it; 1 cites it directly.
4 of 43 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K230152: uMR Omega, Shanghai United Imaging Healthcare Co., Ltd. (2023) Summary page 4.

## Most influential descendants
- K250246: uMR Jupiter (2025), 0 descendants of its own

## Indications for use
uMR Jupiter 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. The device is intended for patients > 20 kg/44 lbs.

Source page: https://510kreport.com/device/K233673
Methodology: https://510kreport.com/methodology