K233673
- 510(k) number
- K233673
- Device name
- uMR Jupiter
- Applicant
- Shanghai United Imaging Healthcare Co., Ltd. CN
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2024-04-26
- Date received
- 2023-11-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K233673.pdf
Official FDA record: K233673
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.