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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 K833268
Device Name ENDOSCOPIC OVERTUBE
Applicant
MILL-ROSE LABORATORY
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
MILL-ROSE LABORATORY
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.1500
Classification Product Code
FED  
Date Received09/21/1983
Decision Date 10/31/1983
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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