# K063021: Profiler 2

- Pathway: 510(k) (Traditional)
- Applicant: Sun Nuclear Corp.
- Decided: Nov 22, 2006 after 51 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K142431: WaterProof PROFILER (2014), 0 descendants of its own

## Indications for use
The Profiler 2 is a device that is designed for use as a radiation scanning system that is used to measure beam data in radiotherapy departments for dose modeling in the treatment planning computer.

Source page: https://510kreport.com/device/K063021
Methodology: https://510kreport.com/methodology