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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 K823103
Device Name DIALYSATE ADDITIVES-POWDER/LIQUID
Applicant
Di-Chem, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Di-Chem, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number876.5820
Classification Product Code
KPO  
Date Received10/20/1982
Decision Date 11/17/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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