# K062163: Mimviewer

- Pathway: 510(k) (Traditional)
- Applicant: Mimvista Corp.
- Decided: Sep 22, 2006 after 56 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K954874 (1996). 32 ancestors in all.
166 later devices descend from it; 3 cite it directly.
0 of 199 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060816: Mim 4.0 (Neuro, Mimvista Corp. (2006) Summary page 1.

## Most influential descendants
- K103785: Mobile Mim (2011), 120 descendants of its own
- K112930: Mobile Mim (2011), 99 descendants of its own
- K151913: MIM-Thin Client (mobile) (2016), 68 descendants of its own
- K172218: MIM – Y90 Dosimetry (2017), 67 descendants of its own
- K070248: Velocityais (2007), 65 descendants of its own

## Indications for use
The MlMviewer software program is used for the registration, fusion and display of medical images from multiple modalities such as SPECT, PET, CT, and MRI. MlMviewer provides tools for image review, manipulation, and analysis that assist physicians both inside and outside the medical environment.

Source page: https://510kreport.com/device/K062163
Methodology: https://510kreport.com/methodology