FDA 510(k) Application Details - K150022

Device Classification Name	Kit, Test, Pregnancy, Hcg, Over The Counter   More FDA Info for this Device
510(K) Number	K150022
Device Name	Kit, Test, Pregnancy, Hcg, Over The Counter
Applicant	Guangzhou Wondfo Biotech Co., Ltd. Wondfo Scientech Park, South China Univ. of technology Guangzhou 510641 CN Other 510(k) Applications for this Company
Contact	Ben Chen Other 510(k) Applications for this Contact
Regulation Number	862.1155   More FDA Info for this Regulation Number
Classification Product Code	LCX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/06/2015
Decision Date	08/07/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review