FDA 510(k) Application Details - K973780

Device Classification Name	Condom   More FDA Info for this Device
510(K) Number	K973780
Device Name	Condom
Applicant	QUALIS, INC. 4600 PARK AVE. DES MOINES, IA 50321 US Other 510(k) Applications for this Company
Contact	MARY A FINN 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	10/03/1997
Decision Date	11/26/1997
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