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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tubes, Gastrointestinal (And Accessories)
510(k) Number K954879
Device Name PERCUTANEOUS REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY (MODIFICATION)
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
9300 PROGRESS PKWY.
MENTOR,  OH  44060
Applicant Contact GRETCHEN YOUNKER
Correspondent
UNITED STATES ENDOSCOPY GROUP, INC.
9300 PROGRESS PKWY.
MENTOR,  OH  44060
Correspondent Contact GRETCHEN YOUNKER
Regulation Number876.5980
Classification Product Code
KNT  
Date Received10/13/1995
Decision Date 03/29/1996
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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