# K932760: DFS-2100

- Pathway: 510(k) (Traditional)
- Applicant: Dba Systems, Inc.
- Decided: Oct 20, 1994 after 499 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K992467: Imagclear Mammography Review System (2000), 2 descendants of its own
- K031132: Consultiva Case Input Station, Model Cis-1 (2003), 1 descendant of its own
- K061160: M-VU Cad Station (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K932760
Methodology: https://510kreport.com/methodology