# K972256: FCR Fuji Computed Radiography DMS CRT Image Console HI-C654 (for Networks)

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: Sep 12, 1997 after 88 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K931002 (1993). 1 ancestor in all.
3 later devices descend from it; 2 cite 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)
- K931002: Fuji Computed Radiograp HI-C654 DMS CRT Image Cons, Fujifilm Medical System U.S.A., Inc. (1993) Summary page 1.

## Most influential descendants
- 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

## Indications for use
The indication for use of the FCR® Fuji Computed Radiography DMS CRT Image Console HI-C654 Multimodality Display System for Networks is to receive, process, display, and transmit medical images.

Source page: https://510kreport.com/device/K972256
Methodology: https://510kreport.com/methodology