# K231273: ArcherQA (V1.0)

- Pathway: 510(k) (Traditional)
- Applicant: Wisdom Technologies., Inc.
- Decided: Jan 5, 2024 after 248 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: 7 generations back to K914698 (1992). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180595: SciMoCa, Radialogica, LLC (2018) Summary page 4.

## Indications for use
ArcherQA is a software product intended to provide quality assurance of a radiation treatment plan generated by a commercial treatment planning system (TPS) by allowing a clinician to re-calculate dose parameters with dose calculation algorithms independent from the commercial TPS and compare the two set of dose information. ArcherQA is not a TPS or a radiation delivery device. It is to be used only by trained radiation oncology personnel for quality assurance purposes.

Source page: https://510kreport.com/device/K231273
Methodology: https://510kreport.com/methodology