FDA 510(k) Application Details - K181722

Device Classification Name	Catheter, Intravascular, Diagnostic   More FDA Info for this Device
510(K) Number	K181722
Device Name	Catheter, Intravascular, Diagnostic
Applicant	Cook Incorporated P.O. Box 489, 750 Daniels Way Bloomington, IN 47402 US Other 510(k) Applications for this Company
Contact	Reuben Lidster Other 510(k) Applications for this Contact
Regulation Number	870.1200   More FDA Info for this Regulation Number
Classification Product Code	DQO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/29/2018
Decision Date	03/22/2019
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