# K023886: Erbe Vio Esu with Accessories, Model Vio 300 D

- Pathway: 510(k) (Special)
- Applicant: Erbe USA, Inc.
- Decided: Dec 12, 2002 after 21 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: 1 generation back to K933002 (1994). 1 ancestor in all.
136 later devices descend from it; 9 cite it directly.
0 of 138 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K933002: Erbotom Icc 350, Erbe USA, Inc. (1994) Summary page 1.

## Most influential descendants
- K060484: Erbe Vio Esu, Model Vio 300 D (2006), 115 descendants of its own
- K083452: Erbe Model Vio 300 D with Accessories (2008), 55 descendants of its own
- K134054: Bovie Ids-310 High Frequency Electrosurgical Generator, Aaron A3350 High Frequency Electrosurgical Generator (2014), 39 descendants of its own
- K110268: Forcetriad Electrosurgical Generator (2011), 16 descendants of its own
- K071728: Modification to: Enseal PTC Tissue Sealing Device (2007), 16 descendants of its own

## Indications for use
High Frequency Electrical Current for the Cutting and/or Coagulation of Tissue

Source page: https://510kreport.com/device/K023886
Methodology: https://510kreport.com/methodology