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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name dialyzer, high permeability with or without sealed dialysate system
510(k) Number K830487
Device Name HEMO-PROCESSING SYSTEM
Applicant
SARTORIUS FILTERS, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
SARTORIUS FILTERS, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number876.5860
Classification Product Code
KDI  
Date Received02/15/1983
Decision Date 04/28/1983
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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