# K892425: STP Complete Module Set

- Pathway: 510(k) (Traditional)
- Applicant: Leibinger & Fischer, Ltd.
- Decided: Mar 23, 1990 after 347 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
25 later devices descend from it; 6 cite it directly.
0 of 26 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
- K961120: Marker System for Stereotaxic Navigation (1996), 17 descendants of its own
- K982463: Extracranial Radiotherapy System (1998), 8 descendants of its own
- K991336: Bodyloc Whole Body Stereotactic Localizer System for Radiotherapy (1999), 7 descendants of its own
- K972324: Leksell Stereotactic System (1998), 7 descendants of its own
- K100691: Omni V SBRT Positioning System, Model RT-4500 (2010), 6 descendants of its own

Source page: https://510kreport.com/device/K892425
Methodology: https://510kreport.com/methodology