FDA 510(k) Application Details - K152507

Device Classification Name	Lubricant, Patient, Vaginal, Latex Compatible   More FDA Info for this Device
510(K) Number	K152507
Device Name	Lubricant, Patient, Vaginal, Latex Compatible
Applicant	DR. AUGUST WOLFF GMBH & CO. KG ARZEIMITTEL SUDBRACKSTR. 56 BIELEFELD 33611 DE Other 510(k) Applications for this Company
Contact	THOMAS FLOETOTTO 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	09/02/2015
Decision Date	05/20/2016
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