# K933129: Lumiscan 50

- Pathway: 510(k) (Traditional)
- Applicant: Lumisys, Inc.
- Decided: Oct 7, 1993 after 101 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; 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
- K982785: Film Digitizer Model 2905 (1998), 1 descendant of its own
- K984252: Imation Trimatic Digital System (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K933129
Methodology: https://510kreport.com/methodology