# K103611: Urology Monopolar Snare for Tissue Transection

- Pathway: 510(k) (Traditional)
- Applicant: United States Endoscopy Group, Inc.
- Decided: May 9, 2011 after 151 days
- Product code: FDI (Snare, Flexible)
- Device class: 2
- Regulation: 21 CFR 876.4300
- 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 K924105 (1992). 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)
- K924105: Snare Flexible, United States Endoscopy Group, Inc. (1992) Summary page 1.
- K923031: Endosnare, Cook Urological, Inc. (1993) Summary page 1.

## Indications for use
The Urology Monopolar Snare for tissue transection is intended to be used in the urological tract for tissue transection for histopathologic examination.

Source page: https://510kreport.com/device/K103611
Methodology: https://510kreport.com/methodology