# K051483: Kodak Directview DR System Detector

- Pathway: 510(k) (Traditional)
- Applicant: Eastman Kodak Company
- Decided: Jun 21, 2005 after 15 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K070829: Synepix 4600 Detector (2007), 0 descendants of its own

## Indications for use
The KODAK DirectView DR System Detector is intended to capture for display radiographic images of human anatomy. It is intended for use in general projection screen-radiographic applications wherever conventional film systems may be used.

Source page: https://510kreport.com/device/K051483
Methodology: https://510kreport.com/methodology