meddevicedb.com FDA Device Reference

Disposable Hemostatic Closure Clip Device

K220157 Class II Traditional
Decision Date
2022-06-13
Sponsor / Applicant
Micro-Tech (Nanjing) Co., Ltd.

Technical Specification

510(k) Submission ID K220157
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2022-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Hemostatic Closure Clip Device received FDA 510(k) clearance under submission number K220157, sponsored by Micro-Tech (Nanjing) 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 2022-06-13.

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.