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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name catheter, cholangiography
510(k) Number K924981
Device Name OPERATIVE CHOLANGIOGRAM CATHETER
Applicant
TAUT, INC.
2571 KANEVILLE COURT
GENEVA,  IL  60134
Applicant Contact KENSETH
Correspondent
TAUT, INC.
2571 KANEVILLE COURT
GENEVA,  IL  60134
Correspondent Contact KENSETH
Regulation Number878.4200
Classification Product Code
GBZ  
Date Received10/01/1992
Decision Date 04/06/1993
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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