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510(k) K160448

ARTLINE by Health Line International Corporation — Product Code DQY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 12, 2016
Date Received
February 18, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Percutaneous
Device Class
Class II
Regulation Number
870.1250
Review Panel
CV
Submission Type

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