# K111833: Virtue

- Pathway: 510(k) (Traditional)
- Applicant: Diagnosoft, Inc.
- Decided: Sep 21, 2011 after 85 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: 4 generations back to K900889 (1990). 6 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023137: Philips Easyvision Workstation Release 6, Philips Medical Systems North America Co. (2002) Summary page 1.
- K100352: Diagnosoft Harp Model 2.06, Diagnosoft, Inc. (2010) Summary page 1.

## Most influential descendants
- K163076: Segment CMR (2017), 2 descendants of its own
- K232007: CAAS MR Solutions (2024), 0 descendants of its own
- K211611: QIR Suite (2022), 0 descendants of its own
- K131158: Corview (2013), 0 descendants of its own

## Indications for use
The Virtue software receives image data from medical scanning devices, such as CT or MRI, or from image archives and performs viewing, image manipulation, communication, printing and quantification of images.

Source page: https://510kreport.com/device/K111833
Methodology: https://510kreport.com/methodology