K251937
- 510(k) number
- K251937
- Device name
- nordicAudio (1.0)
- Applicant
- Nordicneurolab AS NO
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2026-03-20
- Date received
- 2025-06-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K251937.pdf
Official FDA record: K251937
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.