# K931551: Kodak Ektascan Imagelink System (Keis)

- Pathway: 510(k) (Traditional)
- Applicant: Eastman Kodak Company
- Decided: Jun 29, 1993 after 92 days
- Product code: LMD (System, Digital Image Communications, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 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
- K961740: Kodak Digital Science Medical Printer Interface Unit (1996), 0 descendants of its own
- K961739: Kodak Digital Science Medical Modality Acquisition Unit (1996), 0 descendants of its own
- K960382: Kodak Digital Science Medical Image Manager (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K931551
Methodology: https://510kreport.com/methodology