# K931002: Fuji Computed Radiograp HI-C654 DMS CRT Image Cons

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: Jun 8, 1993 after 102 days
- Product code: IXK (System, Imaging, X-Ray, Electrostatic)
- Device class: 2
- Regulation: 21 CFR 892.1630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K972256: FCR Fuji Computed Radiography DMS CRT Image Console HI-C654 (for Networks) (1997), 3 descendants of its own
- K013218: Fuji Speed Suite, Fuji Speed Sute Phase II (2001), 1 descendant of its own
- K091631: Accessnet, Accessmed, Accessrad, Medview (2010), 0 descendants of its own
- K991257: Fuji Wavelet Compression or Ffcomp Irreversible Compression (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K931002
Methodology: https://510kreport.com/methodology