# K241925: VitruvianScan (v1.0)

- Pathway: 510(k) (Traditional)
- Applicant: Perspectum, Ltd.
- Decided: Oct 2, 2024 after 93 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K211983 (2021). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211983: AMRA Profiler, Amra Medical AB (2021) Summary page 5.

## Indications for use
VitruvianScan is indicated for use as a magnetic resonance diagnostic device software application for non-invasive fat and muscle evaluation that enables the generation, display and review of magnetic resonance medical image data. VitruvianScan produces quantified metrics and composite images from magnetic resonance medical image data which when interpreted by a trained healthcare professional, yield information that may assist in clinical decisions.

Source page: https://510kreport.com/device/K241925
Methodology: https://510kreport.com/methodology