# K073670: Kodak Point of Care CR 120, Kodak Point of Care  CR 140, Kodak Point of Care CR 260

- Pathway: 510(k) (Special)
- Applicant: Orex Computed Radiography, Ltd.
- Decided: Jan 25, 2008 after 29 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: 2 generations back to K960834 (1996). 4 ancestors in all.
1 later device descends from it; 1 cites 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)
- K003256: PCCR Digital Imaging Device, Orex Computed Radiography, Ltd. (2000) Summary page 1.
- K032654: Port Cassette, Orex Computed Radiography, Ltd. (2003) Summary page 1.
- K021829: Modification to Kodak Directview CR 800/900 System, Eastman Kodak Company (2002) Summary page 1.

## Most influential descendants
- K192894: Vita Flex CR System with LLI (2020), 0 descendants of its own

## Indications for use
The Point-of-Care is intended for digital radiography using a phosphor storage screen for standard radiographic diagnostic images. The LLI is indicated for Long Length Imaging examinations of long areas of anatomy such as the leg and spine.

Source page: https://510kreport.com/device/K073670
Methodology: https://510kreport.com/methodology