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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name resectoscope, working element
510(k) Number K760174
Device Name ADAPTER, RESECTOSCOPE
Applicant
V. MUELLER O.V. BAXTER HEALTHCARE CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
V. MUELLER O.V. BAXTER HEALTHCARE CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.1500
Classification Product Code
FDC  
Date Received07/06/1976
Decision Date 08/30/1976
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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