FDA 510(k) Application Details - K203818

Device Classification Name	Lubricant, Patient, Vaginal, Latex Compatible   More FDA Info for this Device
510(K) Number	K203818
Device Name	Lubricant, Patient, Vaginal, Latex Compatible
Applicant	Church & Dwight Co., Inc 500 Charles Ewing Blvd. Ewing, NJ 08628 US Other 510(k) Applications for this Company
Contact	Supreet Sahota-Bhatti 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	12/29/2020
Decision Date	06/11/2021
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