# K935928: Rit 113 Film Analysis System

- Pathway: 510(k) (Traditional)
- Applicant: Radiological Imaging Technology, Inc.
- Decided: Jul 29, 1994 after 228 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
48 later devices descend from it; 6 cite it directly.
0 of 49 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K031634: Omnipro I'mrt (2003), 34 descendants of its own
- K072374: Compass (2007), 31 descendants of its own
- K140660: MOBIUS3D (2014), 23 descendants of its own
- K153014: Mobius3D (2016), 13 descendants of its own
- K191761: Mobius3D (2019), 5 descendants of its own

Source page: https://510kreport.com/device/K935928
Methodology: https://510kreport.com/methodology