# K130983: Genii Arc Smart Argon Probe

- Pathway: 510(k) (Traditional)
- Applicant: Genii, Inc.
- Decided: Sep 26, 2013 after 170 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K894762 (1989). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081644: Beamer Argon Probe, Conmed Corporation (2008) Summary page 1.

## Indications for use
The ArC SmartTM Argon Probe is indicated for argon enhanced coagulation of tissue.

Source page: https://510kreport.com/device/K130983
Methodology: https://510kreport.com/methodology