FDA 510(k) Application Details - K961119

Device Classification Name	Pad, Menstrual, Scented   More FDA Info for this Device
510(K) Number	K961119
Device Name	Pad, Menstrual, Scented
Applicant	PERSONAL PRODUCTS CO. 199 GRANDVIEW RD. SKILLMAN, NJ 08558 US Other 510(k) Applications for this Company
Contact	LORNA-JANE BREMER Other 510(k) Applications for this Contact
Regulation Number	884.5425   More FDA Info for this Regulation Number
Classification Product Code	HHL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/21/1996
Decision Date	04/17/1996
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