FDA 510(k) Application Details - K223000

Device Classification Name	More FDA Info for this Device
510(K) Number	K223000
Device Name	Artix BG
Applicant	Inari Medical 6001 Oak Canyon Suite 100 Irvine, CA 92618 US Other 510(k) Applications for this Company
Contact	Ellen Nguyen Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QEW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/28/2022
Decision Date	01/11/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review