FDA 510(k) Application Details - K070830

Device Classification Name	Condom   More FDA Info for this Device
510(K) Number	K070830
Device Name	Condom
Applicant	KAREX INDUSTRIES SDN BHD PTD. 7906/7907, TAMAN PONTIAN JAYA, BT. 34, JALAN JOHOR PONTIAN, JOHOR 82000 MY Other 510(k) Applications for this Company
Contact	LENG KIAN GOH 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	03/26/2007
Decision Date	05/08/2007
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