# K952862: Fuji Computed Radiography System FCR9501ES.FCR

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: Sep 20, 1995 after 90 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
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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
- K122454: Fujifilm Dual Energy Subtraction (Des) Software Option (2012), 6 descendants of its own
- K152244: RADspeed Pro (2016), 3 descendants of its own
- K173517: RADspeed fit (2018), 1 descendant of its own
- K152294: FDR Visionary Suite (2016), 1 descendant of its own
- K233719: FDR Visionary Suite (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K952862
Methodology: https://510kreport.com/methodology