K251822
- 510(k) number
- K251822
- Device name
- MAGNETOM Free.Max; MAGNETOM Free.Star
- Applicant
- Siemens Shenzhen Magnetic Resonance , Ltd. CN
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2025-11-20
- Date received
- 2025-06-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K251822.pdf
Official FDA record: K251822
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.