FDA 510(k) Application Details - K212324

Device Classification Name	Catheter, Intravascular Occluding, Temporary   More FDA Info for this Device
510(K) Number	K212324
Device Name	Catheter, Intravascular Occluding, Temporary
Applicant	RenovoRx, Inc. 4546 El Camino Real, Suite B1 Los Altos, CA 94022 US Other 510(k) Applications for this Company
Contact	Debra Cogan Other 510(k) Applications for this Contact
Regulation Number	870.4450   More FDA Info for this Regulation Number
Classification Product Code	MJN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/26/2021
Decision Date	08/23/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review