FDA 510(k) Application Details - K233913

Device Classification Name	Pump, Breast, Powered   More FDA Info for this Device
510(K) Number	K233913
Device Name	Pump, Breast, Powered
Applicant	AOJ Health Technology Co., Ltd. Rm 302,Block A, Bldg A, Jingfa IntelligentManufacturing Park Xiaweiyuan, Gushu Community,Xixiang Street, Bao'an District Shenzhen 518126 CN Other 510(k) Applications for this Company
Contact	Jack Wang Other 510(k) Applications for this Contact
Regulation Number	884.5160   More FDA Info for this Regulation Number
Classification Product Code	HGX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/12/2023
Decision Date	05/14/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review