# K080715: Erbe Vio Esu, Model Vio 200 S

- Pathway: 510(k) (Special)
- Applicant: Erbe USA, Inc.
- Decided: Apr 2, 2008 after 20 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: 3 generations back to K933002 (1994). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060484: Erbe Vio Esu, Model Vio 300 D, Erbe USA, Inc. (2006) Summary page 1.

## Most influential descendants
- K101108: Erbe Esu Model Vio 100 C with Accessories (2010), 0 descendants of its own

## Indications for use
The ERBE ESU Model VIO 200 S is intended to deliver High Frequency (HF) electrical current for the cutting and/or coagulation of tissue.

Source page: https://510kreport.com/device/K080715
Methodology: https://510kreport.com/methodology