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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 K952982
Device Name ALTREX 110 HEMODIALYZER
Applicant
ALTHIN MEDICAL AB AN AFFILIATE OF BAXTER INTL
14620 N.W. 60TH AVE.
MIAMI LAKES,  FL  33014 -9308
Applicant Contact MARY LANE
Correspondent
ALTHIN MEDICAL AB AN AFFILIATE OF BAXTER INTL
14620 N.W. 60TH AVE.
MIAMI LAKES,  FL  33014 -9308
Correspondent Contact MARY LANE
Regulation Number876.5860
Classification Product Code
KDI  
Date Received06/27/1995
Decision Date 10/05/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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