# K150364: ERBE ESU Model VIO dV with Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Erbe Elektromedizin GmbH
- Decided: May 5, 2016 after 448 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: 5 generations back to K933002 (1994). 5 ancestors in all.
5 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133180: Erbe Esu Model Vio DV with Accessories, Erbe USA, Inc. (2013) Summary page 4.
- K083452: Erbe Model Vio 300 D with Accessories, Erbe USA, Inc. (2008) Summary page 4.

## Most influential descendants
- K191280: E-100 Electrosurgical Generator, SynchroSeal (2019), 4 descendants of its own
- K223039: da Vinci E-200 Electrosurgical Generator (2022), 3 descendants of its own
- K231212: da Vinci E-200 Electrosurgical Generator (2023), 2 descendants of its own
- 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 ERBE ESU Model VIO dV with Accessories is intended to deliver High Frequency (HF) current for the cutting and/or coagulation of tissue.

Source page: https://510kreport.com/device/K150364
Methodology: https://510kreport.com/methodology