FDA 510(k) Application Details - K230372

Device Classification Name	More FDA Info for this Device
510(K) Number	K230372
Device Name	VitreJect Syringe
Applicant	OcuJect, LLC 1441 Avocado Ave, Suite 204 Newport Beach, CA 92660 US Other 510(k) Applications for this Company
Contact	Leonid Lerner Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QLY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/13/2023
Decision Date	09/08/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review