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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 K924643
Device Name MEDTRONIC BIO-MEDICUS CANNULA INSERTION KIT
Applicant
Medtronic Bio-Medicus, Inc.
9600 W. 76th St.
Eden Prairie,  MN  55344
Applicant Contact THOMAS K JOHNSEN
Correspondent
Medtronic Bio-Medicus, Inc.
9600 W. 76th St.
Eden Prairie,  MN  55344
Correspondent Contact THOMAS K JOHNSEN
Regulation Number870.4210
Classification Product Code
DWF  
Date Received09/14/1992
Decision Date 12/08/1992
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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