# K231212: da Vinci E-200 Electrosurgical Generator

- Pathway: 510(k) (Traditional)
- Applicant: Intuitive Surgical
- Decided: Jun 21, 2023 after 54 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: 20 generations back to K930667 (1994). 128 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 131 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K223039: da Vinci E-200 Electrosurgical Generator, Intuitive Surgical (2022) Summary page 4.

## Most influential descendants
- K241635: da Vinci E-200 Electrosurgical Generator (2024), 1 descendant of its own
- K253556: da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator (2026), 0 descendants of its own

## Indications for use
The da Vinci E-200 Electrosurgical Generator is intended to deliver high-frequency energy for cutting, coagulation and vessel sealing of tissues in da Vinci robotic procedures, and non-robotic open and laparoscopic procedures.

Source page: https://510kreport.com/device/K231212
Methodology: https://510kreport.com/methodology