# K192924: MAGNETOM Vida, MAGNETOM Lumina, MAGNETOM Vida Fit

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Mar 11, 2020 after 147 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: 2 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K971684 (1997). 38 ancestors in all.
22 later devices descend from it; 4 cite it directly.
15 of 61 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183254: Magnetom Vida, Siemens Medical Solutions USA, Inc. (2019) Summary page 5.

## Most influential descendants
- K203443: MAGNETOM Vida, MAGNETOM Sola, MAGNETOM Lumina, MAGNETOM Altea (2021), 20 descendants of its own
- K213693: MAGNETOM Vida with syngo MR XA50A (2022), 13 descendants of its own
- K221733: MAGNETOM Sola, MAGNETOM Altea, MAGNETOM Sola Fit (2022), 9 descendants of its own
- K232535: MAGNETOM Sola; MAGNETOM Altea (2023), 4 descendants of its own
- K232482: MAGNETOM Viato.Mobile (2023), 4 descendants of its own

## Recalls of this device
- Aug 28, 2025 · Class I · Z-2658-2025: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, l
- Aug 28, 2025 · Class I · Z-2668-2025: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, l

Source page: https://510kreport.com/device/K192924
Methodology: https://510kreport.com/methodology