FDA 510(k) Application Details - K153372

Device Classification Name	Lubricant, Patient, Vaginal, Latex Compatible   More FDA Info for this Device
510(K) Number	K153372
Device Name	Lubricant, Patient, Vaginal, Latex Compatible
Applicant	FARMA-DERMA S.R.L. VIA DEI BERSAGLIERI,10 SALA BOLOGNESE 40010 IT Other 510(k) Applications for this Company
Contact	MARA CALZOLARI 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	11/23/2015
Decision Date	06/30/2016
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