# K060255: E Surgical Electrosurgical Patient Return Electrode, Dual Plate with Cord and Electrosurgical Patient Return Electrode

- Pathway: 510(k) (Traditional)
- Applicant: E Surgical, LLC
- Decided: Mar 31, 2006 after 58 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) Valleylab, Inc., VL 7600 REM Patient Return Electrode: named in the summary without a submission number

## Most influential descendants
- K071080: Electrosurgical Infant Patient Return Electrode, Dual Plate with Cord, Model EP 211M (2007), 0 descendants of its own

## Indications for use
A single use, non-sterile dispersive electrode with or without a pre-attached cord used to adhere to the patient over the entire pad surface to complete the electrosurgical circuit between the generator, the active electrode, and the patient.

Source page: https://510kreport.com/device/K060255
Methodology: https://510kreport.com/methodology