# K110593: Owl RF Probes

- Pathway: 510(k) (Special)
- Applicant: Diros Technology, Inc.
- Decided: May 5, 2011 after 64 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: 1 generation back to K010202 (2001). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010202: Owl Radiofrequency System, Model Urf-2A, and Associate Radiofrequency Lesion Probes, Leslie W. Organ (2001) Summary page 1.

## Most influential descendants
- K152642: LCCS Disposable RF Electrode, LCCS Reusable RF Electrode (2016), 0 descendants of its own

## Indications for use
The OWL Sterile Single Use Disposable R.F. Probe/Temnperature Sensor is intended for use in Radio-Frequency Heat Lesion procedures for relief of pain.

Source page: https://510kreport.com/device/K110593
Methodology: https://510kreport.com/methodology