FDA 510(k) Application Details - K161898

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K161898
Device Name	Set, Administration, Intravascular
Applicant	BEIJING FERT TECHNOLOGY CO., LTD NO.9, ZHANGGUOZHUANG VILLAGE, CHANGXINDIAN TOWN FENG TAI DISTRICT Beijing 100072 CN Other 510(k) Applications for this Company
Contact	MENG ZHANG Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/11/2016
Decision Date	03/08/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review