# K961740: Kodak Digital Science Medical Printer Interface Unit

- Pathway: 510(k) (Traditional)
- Applicant: Kodak Health Imaging Systems, Inc.
- Decided: Nov 14, 1996 after 195 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- 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 K931551 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K931551: Kodak Ektascan Imagelink System (Keis), Eastman Kodak Company (1993) Summary page 2.

## Indications for use
The KODAK Ektascan Imagelink System (KEIS) is a DICOM conferment product designed for use within a Picture Archiving and Communication System (PACS). The KODAK Ektascan Imagelink System is composed of two major components, the KODAK Digital Science Medical Modality Acquisition Unit and the KODAK Digital Science Medical Printer Interface Unit. These systems can exit together or independently on a network.

Source page: https://510kreport.com/device/K961740
Methodology: https://510kreport.com/methodology