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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, Long-Term Indwelling
510(k) Number K801679
Device Name BETA-CAP II
Applicant
QUINTON, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
QUINTON, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.5630
Classification Product Code
FJS  
Date Received07/22/1980
Decision Date 10/03/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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