FDA 510(k) Application Details - K993870

Device Classification Name	Pad, Menstrual, Unscented   More FDA Info for this Device
510(K) Number	K993870
Device Name	Pad, Menstrual, Unscented
Applicant	PROCTER & GAMBLE CO. 6100 CENTER HILL AVE. CINCINNATI, OH 45224 US Other 510(k) Applications for this Company
Contact	MARK M ANDERSON 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	11/15/1999
Decision Date	01/18/2000
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