FDA 510(k) Application Details - K200508

Device Classification Name	Pump, Breast, Powered   More FDA Info for this Device
510(K) Number	K200508
Device Name	Pump, Breast, Powered
Applicant	Medela LLC 1101 Corporate Drive McHenry, IL 60050 US Other 510(k) Applications for this Company
Contact	PJ Pasia 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	03/02/2020
Decision Date	06/15/2020
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