# K062464: Modification to Autocon II 400 Electrosurgical Generator

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Feb 16, 2007 after 176 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
No predicates in its family tree.
20 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K110268: Forcetriad Electrosurgical Generator (2011), 16 descendants of its own
- K151649: Valleylab FT10 Electrosurgical Platform (2015), 10 descendants of its own
- K170170: Valleylab FT10 Electrosurgical Platform (2017), 8 descendants of its own
- K172757: Valleylab FX8 Electrosurgical Platform (2017), 6 descendants of its own
- K181389: Valleylab FT10 Energy Platform, Valleylab FX8 FX Series Energy Platform (2018), 5 descendants of its own

## Indications for use
The Autocon I 400 Electrosurgical Generator is intended for use by qualified surgeons to provide a high frequency (HF) electrical current for cutting and coagulating tissue.

Source page: https://510kreport.com/device/K062464
Methodology: https://510kreport.com/methodology