meddevicedb.com FDA Device Reference

Disposable Polyp Snare

K220089 Class II Traditional
Decision Date
2022-09-22
Sponsor / Applicant
Jiangsu Vedkang Medical Science and Technology Co., Ltd.

Technical Specification

510(k) Submission ID K220089
Product Code FDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 2022-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Polyp Snare received FDA 510(k) clearance under submission number K220089, sponsored by Jiangsu Vedkang Medical Science and Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2022-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code FDI and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.