FDA 510(k) Application Details - K955648

Device Classification Name	Condom   More FDA Info for this Device
510(K) Number	K955648
Device Name	Condom
Applicant	ORTHO PHARMACEUTICAL CORP. RT. 202 RARITAN, NJ 08869-0602 US Other 510(k) Applications for this Company
Contact	DIANE HERRON 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	12/12/1995
Decision Date	06/21/1996
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