# K152642: LCCS Disposable RF Electrode, LCCS Reusable RF Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Lccs Products Limited
- Decided: Aug 26, 2016 after 346 days
- Product code: GXI (Probe, Radiofrequency Lesion)
- Device class: 2
- Regulation: 21 CFR 882.4725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K010202 (2001). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110593: Owl RF Probes, Diros Technology, Inc. (2011) Summary page 4.
- K010202: Owl Radiofrequency System, Model Urf-2A, and Associate Radiofrequency Lesion Probes, Leslie W. Organ (2001) Summary page 5.

## Indications for use
LCCS Radiofrequency (RF) Electrode is indicated for use in temperature-controlled RF heat lesion procedures of peripheral nerve tissue for the relief of pain.

Source page: https://510kreport.com/device/K152642
Methodology: https://510kreport.com/methodology