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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter, Embolectomy
510(k) Number K233820
Device Name Fogarty Arterial Embolectomy Catheter with Gate Valve
Applicant
Edwards Lifesciences
1 Edwards Way
Irvine,  CA  92614
Applicant Contact Yagna Angirish
Correspondent
Edwards Lifesciences
1 Edwards Way
Irvine,  CA  92614
Correspondent Contact Yagna Angirish
Regulation Number870.5150
Classification Product Code
DXE  
Date Received12/01/2023
Decision Date 05/22/2024
Decision Substantially Equivalent (SESE)
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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