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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name aspiration thrombectomy catheter
510(k) Number K120508
Device Name CLEARLUMEN THROMBECTOMY SYSTEM
Applicant
WALK VASCULAR LLC
17171 DAIMLER ST
IRVINE,  CA  92614
Applicant Contact DAVID LOOK
Correspondent
WALK VASCULAR LLC
17171 DAIMLER ST
IRVINE,  CA  92614
Correspondent Contact DAVID LOOK
Regulation Number870.5150
Classification Product Code
QEZ  
Date Received02/21/2012
Decision Date 11/07/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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