# K070248: Velocityais

- Pathway: 510(k) (Traditional)
- Applicant: Velocity Medical Solutions, LLC
- Decided: Mar 1, 2007 after 35 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). 40 ancestors in all.
65 later devices descend from it; 2 cite it directly.
0 of 106 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010336: Advantage Windows CT/Pet Fusion, Ge Medical Systems, Inc. (2001) Summary page 1.
- K041521: Volume Viewer Plus, General Electric Medical Systems (2004) Summary page 1.
- K062163: Mimviewer, Mimvista Corp. (2006) Summary page 1.

## Most influential descendants
- K081076: Velocityais, Velocity AI, Velocityvx, Velocityrt, V-Response (2008), 63 descendants of its own
- K130393: Mirada RTX (2013), 36 descendants of its own
- K181572: Workflow Box (2018), 25 descendants of its own
- K153014: Mobius3D (2016), 13 descendants of its own
- K173636: Velocity (2018), 8 descendants of its own

## Indications for use
VelocityAlS is a stand-alone software product that provides the physician a means for comparison of medical imaging data from multiple DICOM conformant imaging modality sources. It allows the display, annotating, volume rendering, registration and fusing of medical images as an aid during use by diagnostic radiology, oncology, radiation therapy planning and other medical specialties. VelocityALS is not intended for mammography diagnosis.

Source page: https://510kreport.com/device/K070248
Methodology: https://510kreport.com/methodology