FDA 510(k) Application Details - K180913

Device Classification Name Introducer, Catheter

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510(K) Number K180913
Device Name Introducer, Catheter
Applicant Vascular Solutions, Inc.
6464 Sycamore Court North
Minneapolis, MN 55369 US
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Contact Jake Schultz
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Regulation Number 870.1340

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Classification Product Code DYB
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Date Received 04/09/2018
Decision Date 05/09/2018
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 Y
Expedited Review



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