FDA 510(k) Application Details - K161801

Device Classification Name	Catheter, Continuous Flush   More FDA Info for this Device
510(K) Number	K161801
Device Name	Catheter, Continuous Flush
Applicant	Cook Incorporated 750 Daniels Way Bloomington, IN 47402 US Other 510(k) Applications for this Company
Contact	Jessica Swafford Other 510(k) Applications for this Contact
Regulation Number	870.1210   More FDA Info for this Regulation Number
Classification Product Code	KRA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/30/2016
Decision Date	07/29/2016
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
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