# K062659: Kirwan Disposable Battery-Powered Cautery, Model 41-61XX Series

- Pathway: 510(k) (Traditional)
- Applicant: Kirwan Surgical Products, Inc.
- Decided: Mar 9, 2007 after 183 days
- Product code: HQP (Unit, Cautery, Thermal, Battery-Powered)
- Device class: 2
- Regulation: 21 CFR 886.4115
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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) AAXXX Series, Bovie/Aaron Cautery units: named in the summary without a submission number
- (no number) 844XXXX Series, Medtronic/Solan Cautery units: named in the summary without a submission number
- (no number) 23X Series, Bovie Medical Corp., Perfectemp Cautery units: named in the summary without a submission number

## Indications for use
Kirwan battery-powered cautery units are intended for general surgical use to cauterize small blood vessels in order to help reduce blood loss and keep the site clear of excess blood.

Source page: https://510kreport.com/device/K062659
Methodology: https://510kreport.com/methodology