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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 K140191
Device Name ELISIO-H HEMODIALYZER
Applicant
NIPRO MEDICAL CORPORATION
3150 NW 107 AVE.,
MIAMI,  FL  33172
Applicant Contact CAROLYN GEORGE
Correspondent
NIPRO MEDICAL CORPORATION
3150 NW 107 AVE.,
MIAMI,  FL  33172
Correspondent Contact CAROLYN GEORGE
Regulation Number876.5860
Classification Product Code
KDI  
Date Received01/27/2014
Decision Date 04/14/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
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