# K103665: Conmed R Sabre Genesis TM Electrosurgical Unit; Coned R Sabre Genesis TM Electrosurgical Unit (230V); Conmed Hyfresurg O

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Corporation
- Decided: Feb 16, 2011 after 62 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: 2 generations back to K905654 (1991). 4 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052009: Conmed System Model 2450 Electrosurgical Generator, Conmed Corporation (2005) Summary page 1.
- K020186: Conmed System 5000 Esu, Conmedcorp (2002) Summary page 1.

## Most influential descendants
- K140578: Arthroscopic Energy System (2014), 1 descendant of its own
- K153499: EDGE Arthroscopic Energy System, Arthroscopic Energy System Probes, Arthroscopic Energy System Wireless Footswitch, Arthroscopic Energy System Corded Footswitch, Arthroscopic Energy System Foot Control, Extension (2015), 0 descendants of its own

## Indications for use
General-purpose electrosurgical generator used in conjunction with an electrosurgical accessory handpiece for delivery of RIF (radio frequency) electrosurgical content through an accessory electrode for the cutting and coagulation at the operative site.

Source page: https://510kreport.com/device/K103665
Methodology: https://510kreport.com/methodology