# K220790: Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare

- Pathway: 510(k) (Traditional)
- Applicant: Yangzhou Fartley Medical Instrument Technology Co., Ltd.
- Decided: Jun 27, 2022 after 102 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). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 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.

## Indications for use
Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare is used endoscopically in the removal of diminutive polyps, sessile polyps, pedunculated polyps and tissue from within the GI tract. Disposable Polypectomy Snare shall be used with monopolar diathermic energy. Disposable Polypectomy Hybrid Snare shall be used with or without monopolar diathermic energy.

Source page: https://510kreport.com/device/K220790
Methodology: https://510kreport.com/methodology