FDA 510(k) Application Details - K130569

Device Classification Name	Catheter, Continuous Flush   More FDA Info for this Device
510(K) Number	K130569
Device Name	Catheter, Continuous Flush
Applicant	Translational Research Institute 3420 S MERCY RD #312 GILBERT, AZ 85297 US Other 510(k) Applications for this Company
Contact	DeAnn Dana 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	03/04/2013
Decision Date	11/15/2013
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