FDA 510(k) Application Details - K232930

Device Classification Name	More FDA Info for this Device
510(K) Number	K232930
Device Name	VERVE
Applicant	OculoMotor Technologies 155 Village Blvd, Suite 130 Princeton, NJ 08540 US Other 510(k) Applications for this Company
Contact	Chang Yaramothu, Ph.D. Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	SBN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/20/2023
Decision Date	06/13/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review