# K071343: Ellman Noble Alloy Electrodes

- Pathway: 510(k) (Traditional)
- Applicant: Ellman International, Inc.
- Decided: Feb 28, 2008 after 290 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Ellman Electrodes - Preamendment: named in the summary without a submission number

## Most influential descendants
- K163442: Single Use Micro Electrode (Brass with gold plated shaft); Single Use Micro Electrode (Stainless Steel shaft) (2017), 0 descendants of its own

## Indications for use
The electrodes are accessories to the Ellman electrosurgical generators for cutting of tissue and coagulation by use of high frequency electrical current.

Source page: https://510kreport.com/device/K071343
Methodology: https://510kreport.com/methodology