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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name endoscopic access overtube, gastroenterology-urology
510(k) Number K050253
Device Name USGI SHAPELOCK ENDOSCOPIC GUIDE
Applicant
USGI MEDICAL
1140 CALLE CORDILLERA
SAN CLEMENTE,  CA  92673
Applicant Contact MARY LOU MOONEY
Correspondent
USGI MEDICAL
1140 CALLE CORDILLERA
SAN CLEMENTE,  CA  92673
Correspondent Contact MARY LOU MOONEY
Regulation Number876.1500
Classification Product Code
FED  
Subsequent Product Code
FDF  
Date Received02/03/2005
Decision Date 02/28/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Statement Statement
FDA Review Decision Summary
Type Special
Reviewed by Third Party No
Combination Product No
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