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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Accessory Equipment, Cardiopulmonary Bypass
510(k) Number K841296
Device Name TUBE TENDER
Applicant
THE ANSPACH EFFORT, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
THE ANSPACH EFFORT, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number870.4200
Classification Product Code
KRI  
Date Received03/30/1984
Decision Date 06/11/1984
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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