FDA 510(k) Application Details - K212999

Device Classification Name	Unit, Electrosurgical, Endoscopic (With Or Without Accessories)   More FDA Info for this Device
510(K) Number	K212999
Device Name	Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Applicant	Anrei Medical (Hangzhou) Co., Ltd. No. 3 Ave 8, HEDA Hangzhou 310018 CN Other 510(k) Applications for this Company
Contact	Huibing Yang Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	KNS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/20/2021
Decision Date	03/21/2022
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