# K081678: Conmed Beamer System C600

- Pathway: 510(k) (Abbreviated)
- Applicant: Kls Martin GmbH + Co. KG
- Decided: Jul 29, 2008 after 42 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: 3 generations back to K894762 (1989). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023886: Erbe Vio Esu with Accessories, Model Vio 300 D, Erbe USA, Inc. (2002) Summary page 1.
- K060484: Erbe Vio Esu, Model Vio 300 D, Erbe USA, Inc. (2006) Summary page 1.
- K024047: Erbe Vio Apc with Accessories, Erbe USA, Inc. (2003) Summary page 1.
- K963189: Erbe Apc 300 Argon Plasma Coagulator and Accessories - Argon Plasma Coagulator and Accessories, Erbe USA, Inc. (1996) Summary page 1.
- K013348: Modification to: Erbe Apc Connector Hose and Probes, Models 20132-158, 20132-155, 20132-156, 20132-157, 20132-166, Erbe USA, Inc. (2001)
- K933157: Erbotom Icc 200, Erbe USA, Inc. (1994) Summary page 1.
- K073450: Sutter Electrosurgical Cables, Sutter Medizintechnik GmbH (2008) Summary page 1.

## Most influential descendants
- K122092: Medrange Electrosurgical Expansion System (2012), 0 descendants of its own

## Indications for use
The ConMed Beamer System CE600 with Accessories is intended to deliver electrosurgical current and Argon gas for the cutting, coagulation and argon beam assisted coagulation on tissue when used in conjunction with compatible applicators or probes.

Source page: https://510kreport.com/device/K081678
Methodology: https://510kreport.com/methodology