# K142617: ArcCHECK

- Pathway: 510(k) (Traditional)
- Applicant: Sun Nuclear Corporation
- Decided: Nov 20, 2015 after 430 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
Longest line of descent: 2 generations back to K935928 (1994). 2 ancestors in all.
1 later device descends 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)
- K131466: MAPCHECK2, Arccheck, Sun Nuclear Corporation (2013) Summary page 5.

## Most influential descendants
- K160057: ArcCHECK-MR (2016), 0 descendants of its own

## Indications for use
ArcCHECK, Model 1220 is a three-dimensional (3D) ionizing radiation measurement device intended for radiotherapy quality assurance.

Source page: https://510kreport.com/device/K142617
Methodology: https://510kreport.com/methodology