# K914525: Flurospot H Version 2

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Nov 19, 1991 after 40 days
- Product code: JAA (System, X-Ray, Fluoroscopic, Image-Intensified)
- Device class: 2
- Regulation: 21 CFR 892.1650
- 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; 3 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K961871: Flourospot T.O.P. (1996), 1 descendant of its own
- K954159: Digital Imaging System (1996), 1 descendant of its own
- K023467: HCP Dicom Net (2003), 0 descendants of its own
- K982028: Fluorospot Compact (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K914525
Methodology: https://510kreport.com/methodology