K251386
- 510(k) number
- K251386
- Device name
- ECHELON Synergy
- Applicant
- Fujifilm Corporation JP
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2025-09-17
- Date received
- 2025-05-05
- 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: K251386.pdf
Official FDA record: K251386
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.