# K101686: FDR Image Stitching Option

- Pathway: 510(k) (Special)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: Oct 29, 2010 after 135 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- 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; 3 cite 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
- 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
- K233722: RADspeed Pro (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K101686
Methodology: https://510kreport.com/methodology