# K915362: Vortech's Film Digitizer, FD-1

- Pathway: 510(k) (Traditional)
- Applicant: Vortech Data, Inc.
- Decided: Apr 6, 1992 after 131 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K961768: Kodak Digital Science Film Digitizer L7501/L7506 (with Film Autofeeder) (1996), 1 descendant of its own
- K971894: Kodak Digital Science - Dental Scanning System (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K915362
Methodology: https://510kreport.com/methodology