FDA 510(k) Application Details - K203654

Device Classification Name	Lubricant, Patient, Vaginal, Latex Compatible   More FDA Info for this Device
510(K) Number	K203654
Device Name	Lubricant, Patient, Vaginal, Latex Compatible
Applicant	Solevy Co. LLC 29017 Avenue Penn Santa Clarita, CA 91355 US Other 510(k) Applications for this Company
Contact	Joe Mendoza 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	12/15/2020
Decision Date	04/19/2021
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