FDA 510(k) Application Details - K210124

Device Classification Name	Pump, Breast, Powered   More FDA Info for this Device
510(K) Number	K210124
Device Name	Pump, Breast, Powered
Applicant	Uzinmedicare Co. 56, Dongtansandan 5-Gil,Dongtan-Myeon Hwaseong-Si 18487 KR Other 510(k) Applications for this Company
Contact	Nathan Ahn 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	01/19/2021
Decision Date	10/19/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review