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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 K923529
Device Name DMS DATA MANAGEMENT SYSTEM/DRS-4 DIALYZER REPROCES
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 Received07/16/1992
Decision Date 08/29/1994
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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