# K103785: Mobile Mim

- Pathway: 510(k) (Traditional)
- Applicant: Mim Software, Inc.
- Decided: Feb 4, 2011 after 39 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: 8 generations back to K954874 (1996). 33 ancestors in all.
120 later devices descend from it; 8 cite it directly.
0 of 154 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062163: Mimviewer, Mimvista Corp. (2006) Summary page 1.

## Most influential descendants
- 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
- K180815: MIM - SPECTRA Quant (2018), 54 descendants of its own
- K182624: MIM - MRT Dosimetry (2018), 53 descendants of its own

## Indications for use
The Mobile MIM software program is used for the registration, fusion, and/or display for diagnosis of medical images ftom only the following modalities: SPECT, PET, CT, and MRI. Mobile MIM provides wireless and portable access to medical images. This device is not intended to replace full workstations and should be used only when there is no access to a workstation. This device is not to be used for mammography.

Source page: https://510kreport.com/device/K103785
Methodology: https://510kreport.com/methodology