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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name catheter, continuous irrigation
510(k) Number K872787
Device Name MODIFIED CURLCATH
Applicant
QUINTON, INC.
2121 TERRY AVE.
SEATLE,  WA  98121
Applicant Contact RON R DUCK
Correspondent
QUINTON, INC.
2121 TERRY AVE.
SEATLE,  WA  98121
Correspondent Contact RON R DUCK
Regulation Number878.4200
Classification Product Code
GBQ  
Date Received07/13/1987
Decision Date 08/04/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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