# K960834: Kodak EC-L Cassette

- Pathway: 510(k) (Traditional)
- Applicant: Eastman Kodak Company
- Decided: May 28, 1996 after 89 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K032654: Port Cassette (2003), 4 descendants 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
- 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

Source page: https://510kreport.com/device/K960834
Methodology: https://510kreport.com/methodology