FDA 510(k) Application Details - K071827

Device Classification Name	Pad, Menstrual, Unscented   More FDA Info for this Device
510(K) Number	K071827
Device Name	Pad, Menstrual, Unscented
Applicant	PROCTER & GAMBLE, INC. 6110 CENTER HILL AVENUE CINCINNATI, OH 45224 US Other 510(k) Applications for this Company
Contact	LENORE FAULHABER Other 510(k) Applications for this Contact
Regulation Number	884.5435   More FDA Info for this Regulation Number
Classification Product Code	HHD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/03/2007
Decision Date	09/20/2007
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