FDA 510(k) Application Details - K241680

Device Classification Name	Pump, Breast, Powered   More FDA Info for this Device
510(K) Number	K241680
Device Name	Pump, Breast, Powered
Applicant	Shenzhen Root Innovation Technology Co., Ltd. #2-201, Floor 2, Hasee Computer Building, No. 2 Beier Rd. Bantian Street, Longgang Shenzhen 518129 CN Other 510(k) Applications for this Company
Contact	Audrey Kang 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	06/11/2024
Decision Date	12/20/2024
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