# K980648: Pro Vision

- Pathway: 510(k) (Traditional)
- Applicant: Algotec Systems, Ltd.
- Decided: Jul 20, 1998 after 151 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: 1 generation back to K954678 (1996). 1 ancestor in all.
672 later devices descend from it; 2 cite it directly.
1 of 674 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954678: Pro Vision, Algotec Systems, Ltd. (1996) Summary page 1.

## Most influential descendants
- K992654: Plug 'N View 3D, Version 1.0 (1999), 670 descendants of its own
- K020546: Fusion 7D (2002), 442 descendants of its own
- K022692: Voxelplus Pacs (2002), 252 descendants of its own
- K051528: Mevis Liveranalyser/Liverviewer Software (2005), 226 descendants of its own
- K061696: Iqqa-Liver Software (2006), 217 descendants of its own

## Indications for use
ProVision is an independent diagnostic viewing and processing workstation. It is based on a Silicon Graphics Workstation running under Unix. ProVision communicates with imaging systems of different modalities (currently CT, MRI, CR, RF, NM) utilizing the DICOM - 3 standard. Connection may also be made to any other DICOM device. ProVision functions include: Archiving, displaying, manipulation, filming, 2- and 3-dimensional processing. ProVision employs a graphical multi-Window, icon and mouse driven user interface. It is designed to ensure maxithum flexibility on the one hand, and intuitive operation on the others

Source page: https://510kreport.com/device/K980648
Methodology: https://510kreport.com/methodology