# K914698: Setup Computer with Software V-1261,62 and 63

- Pathway: 510(k) (Traditional)
- Applicant: K.S., Inc.
- Decided: Jun 5, 1992 after 231 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.
124 later devices descend from it; 2 cite it directly.
0 of 125 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K980904: Mucheck Monitor Unit Validation Program (1998), 122 descendants of its own
- K990833: Dose Calc, Model VS. 1.02 (1999), 80 descendants of its own
- K993923: Adac PINNACLE3TM Radiation Therapy Planning System (2000), 79 descendants of its own
- K013112: Focal Sim (2001), 47 descendants of its own
- K032724: PINNACLE3 Radiation Therapy Planning System (2003), 44 descendants of its own

Source page: https://510kreport.com/device/K914698
Methodology: https://510kreport.com/methodology