# K802809: Electron Arc Therapy

- Pathway: 510(k) (Traditional)
- Applicant: Varian Assoc., Inc.
- Decided: Jan 7, 1981 after 61 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.
32 later devices descend from it; 1 cites it directly.
0 of 33 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
- K963258: Peacock System (1996), 31 descendants of its own
- K993766: Helax-TMS V 5.0 Radiation Therapy Treatment Planning System (1999), 24 descendants of its own
- K010682: Helax-TMS V 5.1 Radiation Therapy Treatment Planning System (2001), 23 descendants of its own
- K020971: DCM 2.0 (2002), 22 descendants of its own
- K130617: Raystation (2013), 21 descendants of its own

Source page: https://510kreport.com/device/K802809
Methodology: https://510kreport.com/methodology