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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Dialyzer Reprocessing System
510(k) Number K944539
Device Name DRS 4 ND DIALYZER REPROCESSING SYSTEM
Applicant
SERATRONICS, INC.
2637 SHADELANDS DR.
WALNUT CREEK,  CA  94598
Applicant Contact SCOTT N WALKER
Correspondent
SERATRONICS, INC.
2637 SHADELANDS DR.
WALNUT CREEK,  CA  94598
Correspondent Contact SCOTT N WALKER
Regulation Number876.5820
Classification Product Code
LIF  
Date Received09/15/1994
Decision Date 11/29/1995
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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