K232644
- 510(k) number
- K232644
- Device name
- neuro42 MRI System
- Applicant
- Neuro42, Inc. CA · US
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2024-02-08
- Date received
- 2023-08-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K232644.pdf
Official FDA record: K232644
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.