# K023936: Modification to Mediprime

- Pathway: 510(k) (Special)
- Applicant: Algotec Systems, Ltd.
- Decided: Dec 20, 2002 after 24 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 K002894 (2000). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002894: Mediprime, Algotec Systems, Ltd. (2000) Summary page 1.

## Most influential descendants
- K033013: Mdification to Mediprime (2003), 0 descendants of its own

## Indications for use
The system, that is comprised of diagnostic reading software, is intended for use by radiologists as an interactive tool for analyzing radiological data and generating and viewing radiology reports based on their analysis.

Source page: https://510kreport.com/device/K023936
Methodology: https://510kreport.com/methodology