FDA 510(k) Application Details - K161582

Device Classification Name	Set, Tubing, Blood, With And Without Anti-Regurgitation Valve   More FDA Info for this Device
510(K) Number	K161582
Device Name	Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Applicant	Bain Medical Equipment (Guangzhou) Co., Ltd No. 10 Juncheng Road Eastern Zone of Guangzhou Economic & Technological Guangzhou 510760 CN Other 510(k) Applications for this Company
Contact	Sophia Shao Other 510(k) Applications for this Contact
Regulation Number	876.5820   More FDA Info for this Regulation Number
Classification Product Code	FJK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/08/2016
Decision Date	06/16/2017
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