FDA 510(k) Application Details - K222948

Device Classification Name	More FDA Info for this Device
510(K) Number	K222948
Device Name	Q Distal Access Catheter
Applicant	MIVI Neuroscience, Inc 6545 City West Parkway Eden Prairie, MN 55344 US Other 510(k) Applications for this Company
Contact	Srija Reddy Bandari Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QJP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/27/2022
Decision Date	09/19/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review