FDA 510(k) Application Details - K212180

Device Classification Name	Pump, Breast, Powered   More FDA Info for this Device
510(K) Number	K212180
Device Name	Pump, Breast, Powered
Applicant	Shenzhen TPH Technology Co., Ltd. Bulan Road, Nanwan Community, Longgang District Shenzhen 518100 CN Other 510(k) Applications for this Company
Contact	Peter Chen 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	07/12/2021
Decision Date	02/11/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review