FDA 510(k) Application Details - K960727

Device Classification Name	Pump, Breast, Powered   More FDA Info for this Device
510(K) Number	K960727
Device Name	Pump, Breast, Powered
Applicant	EVENFLO CO., INC. 1333 NEW HAMPSHIRE AVE., N.W. SUITE 400 WASHINGTON, DC 20036 US Other 510(k) Applications for this Company
Contact	DONALD E SEGAL 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	02/22/1996
Decision Date	02/14/1997
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