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510(k) K150894

VIA 21 Microcatheter by Sequent Medical, Inc. — Product Code DQY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 28, 2015
Date Received
April 2, 2015
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

Other clearances by Sequent Medical, Inc.

  • K162565 — VIA 17 Microcatheter (February 18, 2017)
  • K132652 — VIA MICROCATHETER, VIA PLUS MICROCATHETER (December 20, 2013)
  • K123477 — VIA MICROCATHETER, VIA PLUS MICROCATHETER (March 19, 2013)

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