# K141881: Rapidresults

- Pathway: 510(k) (Traditional)
- Applicant: Ramsoft, Inc.
- Decided: Oct 31, 2014 after 112 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 K942120 (1994). 15 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131977: Centricity Universal Viewer Zero Footprint Client, GE Healthcare (2013) Summary page 4.

## Most influential descendants
- K222476: OmegaAI Image Viewer (2022), 3 descendants of its own
- K254237: Cci Pacs Viewer (Pacs-US-001) (2026), 0 descendants of its own
- K241546: aiCockpit AI Viewer (2025), 0 descendants of its own
- K242362: Lightning Viewer (2024), 0 descendants of its own
- K163158: MEDSYNAPSE Zero Footprint Viewer (2016), 0 descendants of its own

## Indications for use
This software displays medical images and associated documents. With appropriate display monitors, lighting, image quality, and level of lossy image compression, the software is intended for use as a primary diagnostic (on desktop platform) and non-diagnostic review tool (on mobile platform) for use by trained healthcare professionals. Each healthcare professional must determine if the level of loss is acceptable for their purpose. This software is not suitable for primary diagnosis of mammograms.

Source page: https://510kreport.com/device/K141881
Methodology: https://510kreport.com/methodology