FDA 510(k) Application Details - K220383

Device Classification Name	Device, Vascular, For Promoting Embolization   More FDA Info for this Device
510(K) Number	K220383
Device Name	Device, Vascular, For Promoting Embolization
Applicant	Okami Medical 8 Argonut Suite 100 Aliso Viejo, CA 92656 US Other 510(k) Applications for this Company
Contact	Jill Delsman Other 510(k) Applications for this Contact
Regulation Number	870.3300   More FDA Info for this Regulation Number
Classification Product Code	KRD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/10/2022
Decision Date	04/29/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review