# K183289: ClearGrasp Snare

- Pathway: 510(k) (Traditional)
- Applicant: Finemedix Co., Ltd.
- Decided: Mar 6, 2019 after 100 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: 5 generations back to K950496 (1995). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K172729: Polypectomy Snare, Hangzhou AGS MedTech Co., Ltd. (2018) Summary page 4.
- K151197: Lariat snare, United States Endoscopy Group, Inc. (2015) Summary page 4.
- K172758: Rotatable Snares, Non-Rotatable Snares, Zhejiang Chuangxiang Medical Technology Co., Ltd. (2018) Summary page 4.

## Most influential descendants
- K220846: Core-Snare (2022), 0 descendants of its own

## Indications for use
The ClearGrasp Snare is used endoscopically in the removal of diminutive polyps, sessile polyps, pedunculated polyps and tissue from within the GI tract.

Source page: https://510kreport.com/device/K183289
Methodology: https://510kreport.com/methodology