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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Gastrointestinal Tubes With Enteral Specific Connectors
510(k) Number K150679
Device Name EndoVive Initial Placement Standard PEG Kit with ENFit Connector, EndoVive Initial Placement Safety PEG Kit with ENFit Connector
Applicant
Boston Scientific Corp
100 Boston Scientific Way
Marlborough,  MA  01756
Applicant Contact Virginia Garcia
Correspondent
Boston Scientific Corp
100 Boston Scientific Way
Marlborough,  MA  01756
Correspondent Contact Virginia Garcia
Regulation Number876.5980
Classification Product Code
PIF  
Date Received03/17/2015
Decision Date 05/29/2015
Decision Substantially Equivalent - Kit With Drugs (SEKD)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product Yes
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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