K241331
- 510(k) number
- K241331
- Device name
- MuscleView
- Applicant
- Springbok, Inc. VA · US
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2024-10-01
- Date received
- 2024-05-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K241331.pdf
Official FDA record: K241331
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.