# K923990: Fuji Computed Radiography HI-C652B DMS CRT Image

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: Dec 17, 1992 after 129 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.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K955643: Alara Imaging System (1996), 4 descendants of its own
- K071682: Crystalview T-Series Computed Radiography System, Models T110 (with Eraser) and T100 (Without Eraser) (2007), 1 descendant of its own
- K974619: Scanaray/CD-Dent Advanced Computerized X-Ray System (1998), 1 descendant of its own
- K102479: Alara T210 Computed Radiography System (2011), 0 descendants of its own
- K990049: CD-Dent Digital Imaging Devices for Dental X-Ray Systems, Models 600, 1000 and 2000 (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K923990
Methodology: https://510kreport.com/methodology