# K971973: Kodak Digital Science Pro-Medical Thermal Printer

- Pathway: 510(k) (Traditional)
- Applicant: Eastman Kodak Company
- Decided: Aug 25, 1997 after 88 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.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The KODAK Digital Science Pro-Medical Thermal Printer is intended to produce continuous tone, photographic quality hard copy output that closely match electronically created or stored images viewed on a CRT display. The device will create either prints or transparencies from digital images acquired from image transmission networks or directly from digital capture or storage devices. The printer accepts digital images in common Raster and POSTSCRIPT formats. The device does not employ any form of lossy data compression.

Source page: https://510kreport.com/device/K971973
Methodology: https://510kreport.com/methodology