# K901423: Digital Image Scanner, Model Dis-1000

- Pathway: 510(k) (Traditional)
- Applicant: Lumisys, Inc.
- Decided: Apr 30, 1990 after 35 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
No predicates in its family tree.
2 later devices descend from it; 2 cite 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
- K973411: Digmi-2000 (Gsi Internal Reference)/LD2800 (Marketing Name) (1997), 1 descendant of its own
- K980565: LD2000 Series (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K901423
Methodology: https://510kreport.com/methodology