# K811230: X-Cell X-Ray #'S P-75W/P-75M

- Pathway: 510(k) (Traditional)
- Applicant: X-Cel X-Ray Corp.
- Decided: Jun 23, 1981 after 50 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K160857: HF 718BD X-Ray System (2017), 2 descendants of its own
- K231761: PodSKAN HF Diagnostic X-ray System (2023), 0 descendants of its own
- K180765: Televere Podiatry X-Ray System HF (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K811230
Methodology: https://510kreport.com/methodology