K232680
- 510(k) number
- K232680
- Device name
- fMRI Hardware System
- Applicant
- Nordicneurolab AS NO
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2023-12-13
- Date received
- 2023-09-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K232680.pdf
Official FDA record: K232680
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.