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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 K942681
Device Name FILTRYZER
Applicant
Toray Industries (America), Inc.
1-1-1 Sonoyama
Otsu-Shi, Shiga-Ken 520,  JP 520
Applicant Contact LISA S JONES
Correspondent
Toray Industries (America), Inc.
1-1-1 Sonoyama
Otsu-Shi, Shiga-Ken 520,  JP 520
Correspondent Contact LISA S JONES
Regulation Number876.5860
Classification Product Code
KDI  
Date Received06/07/1994
Decision Date 06/22/1995
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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