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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 K013713
Device Name ARM AUTOMATIC REPROCESSING MACHINE
Applicant
Alcavis International Incorporated
8-8 Metropolitan Ct.
Gaithersburg,  MD  20878
Applicant Contact LUDOVICO GIAVOTTO
Correspondent
Alcavis International Incorporated
8-8 Metropolitan Ct.
Gaithersburg,  MD  20878
Correspondent Contact LUDOVICO GIAVOTTO
Regulation Number876.5820
Classification Product Code
LIF  
Date Received11/08/2001
Decision Date 07/15/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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