K241925
- 510(k) number
- K241925
- Device name
- VitruvianScan (v1.0)
- Applicant
- Perspectum, Ltd. GB
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2024-10-02
- Date received
- 2024-07-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K241925.pdf
Official FDA record: K241925
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.