K232322
- 510(k) number
- K232322
- Device name
- MAGNETOM Terra; MAGNETOM Terra.X
- Applicant
- Siemens Medical Solutions USA, Inc. PA · US
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2024-03-22
- Date received
- 2023-08-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K232322.pdf
Official FDA record: K232322
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.