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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 K140296
Device Name CLEARLUMEN THROMBECTOMY SYSTEM
Applicant
Walk Vascular, LLC
17171 Daimler St.
Irvine,  CA  92614
Applicant Contact BRAD CULBERT
Correspondent
Walk Vascular, LLC
17171 Daimler St.
Irvine,  CA  92614
Correspondent Contact Brad Culbert
Regulation Number870.5150
Classification Product Code
QEZ  
Date Received02/06/2014
Decision Date 12/02/2014
Decision SE - With Limitations (SESU)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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