# K053183: Jive X Software

- Pathway: 510(k) (Traditional)
- Applicant: Visus Technology Transfer GmbH
- Decided: Feb 16, 2006 after 94 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
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K142750: JiveX (2015), 6 descendants of its own
- K162008: JiveX (2016), 4 descendants of its own
- K181964: JiveX (2018), 3 descendants of its own
- K200703: JiveX (2020), 2 descendants of its own
- K212321: JiveX (Model Number / Release: 5.3) (2021), 1 descendant of its own

## Indications for use
To be used with images from a variety of radiological modalities including CT, MRI, ultrasound, nuclear medicine, CR, DR, etc. to store and retrieve images and patient information. Lossy compressed mammographic images and digitized film screen images must not be reviewed for primary image interpretations. Mammographic images may only be interpreted us;i': :n FDA approved monitor that offers at least 5 Mpixel resolution and meets other technical specifications reviewed and accepted by FDA.

Source page: https://510kreport.com/device/K053183
Methodology: https://510kreport.com/methodology