# K974086: Kodak Digital Science Cardiac Viewer

- Pathway: 510(k) (Traditional)
- Applicant: Eastman Kodak Company
- Decided: Jan 20, 1998 after 83 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K992575: Cardiovascular Workstation, Model CWS 5000/CWS 3000 (1999), 0 descendants of its own

## Indications for use
The software, when installed on PC-based system, enables the medical professional to read Angiographic and Cardiac patient exam records from pre-recorded, transferable media (i.e., CD-R), magnetic hard disc drives and networks. The software enables motion files to be viewed at speeds of up to 60 frames per second, at slow speeds and as still frames. The software enables the printing of still frames as well as the exporting of both still and dynamic patient exam files and will be marked “For referral use only” when appropriate.

Source page: https://510kreport.com/device/K974086
Methodology: https://510kreport.com/methodology