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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name system, dialysate delivery, single patient
510(k) Number K761287
Device Name 5M1352 PROPORT. DIALYSIS FLUID DELIV.ERY
Applicant
TRAVENOL LABORATORIES, S.A.
803 N. Front St. Suite 3
mchenry,  IL  60050
Correspondent
TRAVENOL LABORATORIES, S.A.
803 N. Front St. Suite 3
mchenry,  IL  60050
Regulation Number876.5820
Classification Product Code
FKP  
Date Received12/20/1976
Decision Date 01/03/1977
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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