# K221945: Beamer AVEO FILTER INTEGRATED ARGON PROBE 1.8mm x 160 cm, Beamer AVEO FILTER INTEGRATED ARGON PROBE 1.8 mm X 320 cm, Beamer AVEO FILTER INTEGRATED ARGON PROBE 2.3 mm X 230 cm, Beamer AVEO FILTER INTEGRATED ARGON PROBE 2.3 mm x 320 cm, Beamer AVEO FILTER INTEGRATED ARGON SIDEFIRE PROBE 2.3 mm x 230 cm

- Pathway: 510(k) (Special)
- Applicant: Conmed Corporation
- Decided: Jul 28, 2022 after 23 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 4.

## Indications for use
The Beamer AVEOTM Filter Integrated Argon Probes and Beamer AVEOTM Filter Integrated Argon SideFire Probe are intended to be used for argon enhanced coagulation of tissue.

Source page: https://510kreport.com/device/K221945
Methodology: https://510kreport.com/methodology