# K042386: Direct Digitizer, Regius Model 190

- Pathway: 510(k) (Special)
- Applicant: Konica Minolta Medical & Graphic, Inc.
- Decided: Dec 15, 2004 after 104 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- Device class: 2
- Regulation: 21 CFR 892.1680
- 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 K023061 (2002). 1 ancestor in all.
5 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023061: Konica Direct Digitizer Regius, Model 170, Konica Minolta Medical & Graphic, Inc. (2002) Summary page 1.

## Most influential descendants
- K052095: Modification to: Direct Digitizer Regius Model 190 (2005), 4 descendants of its own
- K071181: Direct Digitizer, Regius Model 110 (2007), 2 descendants of its own
- K103703: Reguis Sigma (2011), 1 descendant of its own
- K120131: Regius SIGMA2 (2012), 0 descendants of its own
- K092717: Direct Digitizer, Regius Model 210 (2009), 0 descendants of its own

## Indications for use
The Direct Digitizer, REGIUS Model 190 is an X-ray image reader which uses a stimulable phosphor plate (Plate) as X-ray detector installed in a separate cassette. It reads the image recorded on the Plate and transfers the image data to an externally connected device such as a host computer, an order input device, an image display device, a printer, an image data filing device, and other image reproduction devices. It is designed and intended to be used by trained medical personnel in a clinic, a radiology department in a hospital and in other medical facilities. This device is not intended for use with digital mammography system.

Source page: https://510kreport.com/device/K042386
Methodology: https://510kreport.com/methodology