# K003256: PCCR Digital Imaging Device

- Pathway: 510(k) (Traditional)
- Applicant: Orex Computed Radiography, Ltd.
- Decided: Nov 8, 2000 after 22 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.
5 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K052938: CR-PRO (2005), 2 descendants of its own
- K142718: Radlink GPS (2014), 1 descendant of its own
- K073670: Kodak Point of Care CR 120, Kodak Point of Care  CR 140, Kodak Point of Care CR 260 (2008), 1 descendant of its own
- K242161: Radlink GPS Pro Imaging (2025), 0 descendants of its own
- K192894: Vita Flex CR System with LLI (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K003256
Methodology: https://510kreport.com/methodology