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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name set, administration, for peritoneal dialysis, disposable
510(k) Number K860700
Device Name CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186
Applicant
TRAVENOL LABORATORIES, S.A.
DEERFIELD,  IL  60015
Applicant Contact JULIA A MEYER
Correspondent
TRAVENOL LABORATORIES, S.A.
DEERFIELD,  IL  60015
Correspondent Contact JULIA A MEYER
Regulation Number876.5630
Classification Product Code
KDJ  
Date Received02/25/1986
Decision Date 04/07/1986
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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