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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 K992141
Device Name OLYMPUS WORKING ELEMENT FOR PROBES
Applicant
OLYMPUS WINTER & IBE GMBH
TWO CORPORATE CENTER DR.
MELVILLE,  NY  11747 -3157
Applicant Contact LAURA STORMS-TYLER
Correspondent
OLYMPUS WINTER & IBE GMBH
TWO CORPORATE CENTER DR.
MELVILLE,  NY  11747 -3157
Correspondent Contact LAURA STORMS-TYLER
Regulation Number876.1500
Classification Product Code
FDC  
Date Received06/24/1999
Decision Date 09/29/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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