# K112930: Mobile Mim

- Pathway: 510(k) (Traditional)
- Applicant: Mim Software, Inc.
- Decided: Dec 2, 2011 after 60 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: 9 generations back to K954874 (1996). 37 ancestors in all.
99 later devices descend from it; 6 cite it directly.
0 of 137 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K103785: Mobile Mim, Mim Software, Inc. (2011) Summary page 1.
- K042956: Vision, Varian Medical Systems, Inc. (2005) Summary page 1.

## Most influential descendants
- 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
- K191928: AccuContour (2020), 30 descendants of its own

## Indications for use
The Mobile MIM software program is used for the viewing, registration, fusion, and/or display for diagnosis of medical images from the following modalities: SPECT, PET, CT, MRI, X-ray and Ultrasound. Mobile MIM can be used to review images, contours, DVH, and isodose curves from radiation treatment plans. Mobile MIM can be used to approve these plans. 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/K112930
Methodology: https://510kreport.com/methodology