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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Dialysate Delivery, Central Multiple Patient
510(k) Number K844756
Device Name ST FAMILY OF HOLLOW FIBER DIALYZERS
Applicant
Travenol Laboratories, S.A.
Deerfield,  IL  60015
Applicant Contact JULIA A MEYER
Correspondent
Travenol Laboratories, S.A.
Deerfield,  IL  60015
Correspondent Contact JULIA A MEYER
Regulation Number876.5820
Classification Product Code
FKQ  
Date Received12/05/1984
Decision Date 01/16/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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