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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name catheter, peritoneal dialysis, single use
510(k) Number K871730
Device Name MODIFIED USE OF PULL-APART INTRODUCER SET
Applicant
QUINTON, INC.
2121 TERRY AVE.
SEATLE,  WA  98121
Applicant Contact MAYR-LEE DONOGHUE
Correspondent
QUINTON, INC.
2121 TERRY AVE.
SEATLE,  WA  98121
Correspondent Contact MAYR-LEE DONOGHUE
Regulation Number876.5630
Classification Product Code
FKO  
Date Received05/05/1987
Decision Date 05/18/1987
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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