# K082347: Digital Radiography, Flexdr C30

- Pathway: 510(k) (Traditional)
- Applicant: Konica Minolta Technoproduct Co., Ltd.
- Decided: Nov 18, 2008 after 95 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: 4 generations back to K981556 (1998). 5 ancestors in all.
23 later devices descend from it; 1 cites it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051418: Direct Digitizer Regius  Model 370, Konica Minolta Medical & Graphic, Inc. (2005) Summary page 1.
- K031633: Canon Inc., Digital Radiography, Model Cxdi-40C, Canon USA, Inc. (2003) Summary page 1.

## Most influential descendants
- K102349: Aerodr System (2010), 22 descendants of its own
- K120477: Aerosync for Aerodr System (2012), 14 descendants of its own
- K113248: Aerodr System with P-21 (2012), 14 descendants of its own
- K130936: Aerodr System with P-31 (2013), 13 descendants of its own
- K141271: Aerodr System 2 (2014), 12 descendants of its own

## Indications for use
The device is intended for use for medical purpose in a hospital, etc., in order to convert X-ray image data to digital signal and to transfer the converted data to printer, filing system, image display device, etc. Flex DR C30 is not intended for use with FFDM systems.

Source page: https://510kreport.com/device/K082347
Methodology: https://510kreport.com/methodology