FDA 510(k) Application Details - K230363

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K230363
Device Name	Catheter, Percutaneous
Applicant	CenterPoint Systems LLC 3338 Parkway Blvd West Valley City, UT 84119 US Other 510(k) Applications for this Company
Contact	Marybeth Gamber 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	02/10/2023
Decision Date	03/09/2023
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