# K060137: Kodak Eclipse Image Processing Software

- Pathway: 510(k) (Special)
- Applicant: Eastman Kodak Company
- Decided: Mar 16, 2006 after 56 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.
9 later devices descend from it; 5 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K180809: Eclipse II (2018), 2 descendants of its own
- K100094: Carestream Image Suite (2010), 2 descendants of its own
- K202441: Eclipse II with Smart Noise Cancellation (2021), 1 descendant of its own
- K140271: Tablet Viewer Software for Image Suite (2014), 1 descendant of its own
- K251168: Image Suite (2025), 0 descendants of its own

## Indications for use
The CR Systems are compact laser scanners capable of reading the latent image formed on a storage phosphor imaging plate and producing a digital image for projection radiography applications. This excludes mammography applications for the Kodak Ektascan Storage Phosphor Reader and the Kodak Eclipse image Processing Software in the United States.

Source page: https://510kreport.com/device/K060137
Methodology: https://510kreport.com/methodology