K242825
- 510(k) number
- K242825
- Device name
- Prenuvo Body Composition
- Applicant
- Prenuvo CA · US
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2025-01-17
- Date received
- 2024-09-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K242825
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.