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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name dialyzer, capillary, hollow fiber
510(k) Number K782151
Device Name ARTIFICIAL KIDNEY, C-DAK 0.6D
Applicant
CORDIS CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
CORDIS CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.5820
Classification Product Code
FJI  
Date Received12/26/1978
Decision Date 02/22/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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