FDA 510(k) Application Details - K221713

Device Classification Name	Snare, Flexible   More FDA Info for this Device
510(K) Number	K221713
Device Name	Snare, Flexible
Applicant	Hangzhou AGS MedTech Co., Ltd. Building 5, Building 6, No. 597 Kangxin Road Yuhang District Hangzhou 311106 CN Other 510(k) Applications for this Company
Contact	Jiayuan Zhang Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	FDI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/13/2022
Decision Date	03/03/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review