FDA 510(k) Application Details - K243421

Device Classification Name	Condom   More FDA Info for this Device
510(K) Number	K243421
Device Name	Condom
Applicant	Lelo Inc. 5799 Fontanoso Way San Jose, CA 95138 US Other 510(k) Applications for this Company
Contact	Pavle Sedic Other 510(k) Applications for this Contact
Regulation Number	884.5300   More FDA Info for this Regulation Number
Classification Product Code	HIS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/04/2024
Decision Date	03/07/2025
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