# K132136: Single Use Grounding Pad

- Pathway: 510(k) (Traditional)
- Applicant: Lccs Products Limited
- Decided: Sep 6, 2013 after 57 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 K954633 (1995). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120476: Macrolyte Dispersive Electrode, Conmed Corporation (2012) Summary page 1.
- K052878: NT-1000, Neuro Therm, Inc. (2006) Summary page 1.

## Indications for use
The Single Use Grounding Pad Is applied to the patient during electrosurgical procedures to provide a path for the RF current to leave the patient and return to the generator.

Source page: https://510kreport.com/device/K132136
Methodology: https://510kreport.com/methodology