# K231126: Eblator Device

- Pathway: 510(k) (Traditional)
- Applicant: E Surgical, LLC
- Decided: Aug 2, 2023 after 104 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: 16 generations back to K011083 (2001). 81 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 83 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K152777: Bovie Disposable Bipolar Ablator, Bovie Medical Corporation (2016) Summary page 4.
- K161558: Bovie 3.3mm Disposable Bipolar Ablator 90°, Aspirating and Non-Aspirating, Bovie 2.4mm Disposable Bipolar Ablator 55°, Non-Aspirating,  Bovie 1.8mm Disposable Bipolar Ablator 60°, Non-Aspirating, Bovie Medical Corporation (2016) Summary page 4.

## Most influential descendants
- K251899: E Blator (2025), 0 descendants of its own

## Indications for use
The Eblator Device is intended for general arthroscopic applications, which include cutting, vaporization, and coagulation. This device is intended to be used in conjunction with a general purpose electrosurgical generator via a standard active lead and a standard return lead connection. The device is only operable when activated in an appropriate conductive media, such as a standard saline solution.

Source page: https://510kreport.com/device/K231126
Methodology: https://510kreport.com/methodology