FDA 510(k) Application Details - K152381

Device Classification Name Introducer, Catheter

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510(K) Number K152381
Device Name Introducer, Catheter
Applicant MERIT MEDICAL SYSTEMS, INC.
65 GREAT VALLEY PARKWAY
MALVERN, PA 19355 US
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Contact Alina Stubbs
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Regulation Number 870.1340

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Classification Product Code DYB
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Date Received 08/24/2015
Decision Date 10/30/2015
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review



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