# K183148: OKLand Patient Return Electrode Pad

- Pathway: 510(k) (Traditional)
- Applicant: Auckland Medical Polymer (Tianjin) Co., Ltd.
- Decided: Feb 4, 2020 after 448 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: 7 generations back to K822572 (1982). 17 ancestors in all.
No later device cites it as a predicate yet.
5 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133726: Mega Soft Universal Patient Return Electrode, Megadyne Medical Products, Inc. (2014) Summary page 4.

## Indications for use
OKLand Patient Return Electrode Pad is designed to be used whenever monopolar electrosurgery is indicated. The intended use of this device is to conduct monopolar electrosurgical energy from target tissue of a patient back to one or two electrosurgical units (ESU) or generators in monopolar surgery. This device is restricted to use with isolated monopolar electrosurgical generators, not intended for radio frequency ablation.

Source page: https://510kreport.com/device/K183148
Methodology: https://510kreport.com/methodology