K231617
- 510(k) number
- K231617
- Device name
- MAGNETOM Free.Max; MAGNETOM Free.Star
- Applicant
- Siemens Medical Solutions USA, Inc. PA · US
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2023-11-09
- Date received
- 2023-06-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K231617.pdf
Official FDA record: K231617
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.