meddevicedb.com FDA Device Reference

Haemostasis Clips

K241005 Class II Traditional
Decision Date
2025-01-02
Sponsor / Applicant
Jiangxi Zhuoruihua Medical Instrument Co., Ltd.

Technical Specification

510(k) Submission ID K241005
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2025-01-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Haemostasis Clips received FDA 510(k) clearance under submission number K241005, sponsored by Jiangxi Zhuoruihua Medical Instrument 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 2025-01-02.

Classification & Regulation

This clearance is catalogued under FDA product code PKL and 21 CFR 876.4400, within the Gastroenterology, Urology review panel as a Class II device.