# K061884: Bovie Icon GI Electrosurgical Generator, Model GI 120

- Pathway: 510(k) (Traditional)
- Applicant: Bovie Medical
- Decided: Sep 6, 2006 after 65 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 K944602 (1995). 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)
- K022856: Bovie Ids-300 High Frequency Electrosurgical Generator, Aaron Medical Industries (2003) Summary page 1.
- K933157: Erbotom Icc 200, Erbe USA, Inc. (1994) Summary page 1.

## Most influential descendants
- K082109: Bovie Icon General Purpose RF Generator (2008), 1 descendant of its own
- K092383: Bovie Icon VS General Purpose RF Generator, Model: VS300 (2010), 0 descendants of its own

## Indications for use
The Bovie ICON GI Generator is used to deliver high frequency radiofrequency energy in conjunction with other surgical devices to cut and coagulate different kinds of tissues.

Source page: https://510kreport.com/device/K061884
Methodology: https://510kreport.com/methodology