FDA 510(k) Application Details - K233350

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K233350
Device Name	Catheter, Percutaneous
Applicant	Reflow Medical, Inc. 208 Avenida Fabricante #100 San Clemente, CA 92672 US Other 510(k) Applications for this Company
Contact	Lori Grace Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	DQY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2023
Decision Date	02/08/2024
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