FDA 510(k) Application Details - K972836

Device Classification Name	Condom With Nonoxynol-9   More FDA Info for this Device
510(K) Number	K972836
Device Name	Condom With Nonoxynol-9
Applicant	G. PREMJEE (USA), INC. 55 NORTHER BLVD. SUITE 410 GREAT NECK, NY 11021 US Other 510(k) Applications for this Company
Contact	SUSAN D GOLDSTEIN-FALK Other 510(k) Applications for this Contact
Regulation Number	884.5310   More FDA Info for this Regulation Number
Classification Product Code	LTZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/31/1997
Decision Date	10/22/1997
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