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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 K926005
Device Name FRESENIUS HEMOFLOW, VARIOUS MODELS
Applicant
FRESENIUS USA, INC.
2637 SHADELANDS DR.
WALNUT CREEK,  CA  94598
Applicant Contact SCOTT N WALKER
Correspondent
FRESENIUS USA, INC.
2637 SHADELANDS DR.
WALNUT CREEK,  CA  94598
Correspondent Contact SCOTT N WALKER
Regulation Number876.5820
Classification Product Code
FJI  
Subsequent Product Code
KDI  
Date Received11/27/1992
Decision Date 08/23/1994
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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