FDA 510(k) Application Details - K231786

Device Classification Name	Pessary, Vaginal   More FDA Info for this Device
510(K) Number	K231786
Device Name	Pessary, Vaginal
Applicant	Cosm Medical 101 College Street Toronto M5G1L7 CA Other 510(k) Applications for this Company
Contact	Linda Wu Other 510(k) Applications for this Contact
Regulation Number	884.3575   More FDA Info for this Regulation Number
Classification Product Code	HHW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/2023
Decision Date	03/06/2024
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