# K032654: Port Cassette

- Pathway: 510(k) (Traditional)
- Applicant: Orex Computed Radiography, Ltd.
- Decided: Oct 9, 2003 after 42 days
- Product code: IXK (System, Imaging, X-Ray, Electrostatic)
- Device class: 2
- Regulation: 21 CFR 892.1630
- 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 K960834 (1996). 1 ancestor in all.
4 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)
- K960834: Kodak EC-L Cassette, Eastman Kodak Company (1996) Summary page 1.

## Most influential descendants
- 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
- K042779: Radiotherapy Solution Based on CR (2004), 1 descendant of its own
- K192894: Vita Flex CR System with LLI (2020), 0 descendants of its own
- K070920: Fuji IP Cassette Type PC (2007), 0 descendants of its own

## Indications for use
The PoRT Cassette is an accessory to the PcCR Digital Imaging Device and is indicated for portal imaging (Radiation Therapy Quality Control).

Source page: https://510kreport.com/device/K032654
Methodology: https://510kreport.com/methodology