# K971894: Kodak Digital Science - Dental Scanning System

- Pathway: 510(k) (Traditional)
- Applicant: Eastman Kodak Company
- Decided: Aug 20, 1997 after 90 days
- Product code: LMA (Digitizer, Image, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K930527 (1993). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K961768: Kodak Digital Science Film Digitizer L7501/L7506 (with Film Autofeeder), Kodak Health Imaging Systems, Inc. (1996) Summary page 1.
- K955237: Tigerscan/Tigerview, Tau Corp. (1996) Summary page 1.

## Indications for use
Scanning of dental radiographic film

Source page: https://510kreport.com/device/K971894
Methodology: https://510kreport.com/methodology