FDA 510(k) Application Details - K071313

Device Classification Name	Condom   More FDA Info for this Device
510(K) Number	K071313
Device Name	Condom
Applicant	CHURCH & DWIGHT CO., INC. 469 NORTH HARRISON STREET PRINCETON, NJ 08543 US Other 510(k) Applications for this Company
Contact	STEPHEN C KOLAKOWSKY Other 510(k) Applications for this Contact
Regulation Number	884.5300   More FDA Info for this Regulation Number
Classification Product Code	HIS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/10/2007
Decision Date	10/26/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review