# K051521: Regius RS-1000, Medical Image Processing Workstation

- Pathway: 510(k) (Traditional)
- Applicant: Konica Minolta Medical & Graphic, Inc.
- Decided: Jun 28, 2005 after 20 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 K041990 (2004). 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)
- K041990: Fuji Medical CR Console, Model Flash Iip, Fujifilm Medical System U.S.A., Inc. (2004) Summary page 4.

## Most influential descendants
- K060210: Mediport (2006), 0 descendants of its own

## Indications for use
Receive and process electronic images of patients. The REGIUS RS-1000 is NOT intended for use with digital mammography system.

Source page: https://510kreport.com/device/K051521
Methodology: https://510kreport.com/methodology