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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name electrode, electrosurgical, active, urological
510(k) Number K102781
Device Name RESECTION BUTTON ELECTRODE FOR PLASMA VAPORIZATION, HF-RESECTION ELECTRODE ROLLERS AND NEEDLES, LOOPS AND BANDS
Applicant
OLYMPUS WINTER & IBE GMBH
3500 CORPORATE PKWAY
PO BOX 610
CENTER VALLEY,  PA  18034 -0610
Applicant Contact STACY ABBATIELLO
Correspondent
OLYMPUS WINTER & IBE GMBH
3500 CORPORATE PKWAY
PO BOX 610
CENTER VALLEY,  PA  18034 -0610
Correspondent Contact STACY ABBATIELLO
Regulation Number876.4300
Classification Product Code
FAS  
Subsequent Product Code
GEI  
Date Received09/27/2010
Decision Date 01/11/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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