FDA 510(k) Application Details - K193197

Device Classification Name

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510(K) Number K193197
Device Name QuickClear Mechanical Thrombectomy System
Applicant Volcano AtheroMed Inc.
1530 O'Brien Drive, Suite A
Menlo Park, CA 94025 US
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Contact Anna Gloria Stephen
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Regulation Number

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Classification Product Code QEZ
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Date Received 11/20/2019
Decision Date 04/20/2020
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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