FDA 510(k) Application Details - K131084

Device Classification Name	Lubricant, Patient, Vaginal, Latex Compatible   More FDA Info for this Device
510(K) Number	K131084
Device Name	Lubricant, Patient, Vaginal, Latex Compatible
Applicant	SASMAR INC 155 NORTH WACKER DR, STE 4250 CHICAGO, IL 60606 US Other 510(k) Applications for this Company
Contact	JOHN-MICHAEL MANCINI Other 510(k) Applications for this Contact
Regulation Number	884.5300   More FDA Info for this Regulation Number
Classification Product Code	NUC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/18/2013
Decision Date	09/13/2013
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