meddevicedb.com FDA Device Reference

Disposable Trocar

K202931 Class II Traditional
Decision Date
2020-11-17
Sponsor / Applicant
Wuxi Shukang Medical Appliance Co., Ltd.

Technical Specification

510(k) Submission ID K202931
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2020-11-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Trocar received FDA 510(k) clearance under submission number K202931, sponsored by Wuxi Shukang Medical Appliance 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 2020-11-17.

Classification & Regulation

This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.