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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 K830284
Device Name FH 101, FH 202 & FH 303 FIBER HEMOFILTER
Applicant
GAMBRO, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
GAMBRO, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.5860
Classification Product Code
KDI  
Date Received01/27/1983
Decision Date 03/02/1983
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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