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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name dialysate concentrate for hemodialysis (liquid or powder)
510(k) Number K911459
Device Name GRANULYTE POWDER DIALYSATE CONCENTRATE AND MIXING
Original Applicant
FRESENIUS USA, INC.
4090 pike ln.
concord,  CA  94520
Original Contact tom folden
Regulation Number876.5820
Classification Product Code
KPO  
Date Received04/03/1991
Decision Date 07/17/1991
Decision substantially equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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