# K901956: Digital 8 W/Other Numerical Suffixes (1-9, Etc.)

- Pathway: 510(k) (Traditional)
- Applicant: Eigen
- Decided: Jul 2, 1990 after 62 days
- Product code: LMB (Device, Digital Image Storage, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2010
- 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
- K063846: Eigen Dsa 2000 (2007), 1 descendant of its own
- K082341: DSA 2000EX (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K901956
Methodology: https://510kreport.com/methodology