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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
510(k) Number K770068
Device Name CANNULA, HUNTER-SESSIONS, SELF-RETAIN.
Applicant
Barlow Mfg., Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Barlow Mfg., Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.4210
Classification Product Code
DWF  
Date Received01/12/1977
Decision Date 03/01/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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