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510(k) K071468

CLARIVEIN CATHETER by Vascular Insights, LLC — Product Code KRA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 20, 2008
Date Received
May 29, 2007
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Continuous Flush
Device Class
Class II
Regulation Number
870.1210
Review Panel
CV
Submission Type

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