FDA 510(k) Application Details - K102714

Device Classification Name Device, Vascular, For Promoting Embolization

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510(K) Number K102714
Device Name Device, Vascular, For Promoting Embolization
Applicant BOSTON SCIENTIFIC CORP.
ONE SCIMED PLACE
MAPLE GROVE, MN 55311 US
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Contact DEBBIE MCINTIRE
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Regulation Number 870.3300

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Classification Product Code KRD
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Date Received 09/20/2010
Decision Date 02/11/2011
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 N
Expedited Review



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