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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name electrosurgical, cutting & coagulation & accessories
510(k) Number K062082
Device Name CONMED ABC DISSECTING BLADE ELECTRODE, MODEL 139330; BLUNT NEEDLE ELECTRODE, MODEL 139331
Applicant
CONMED CORPORATION
14603 E. FREMONT AVE.
CENTENNIAL,  CO  80112
Applicant Contact SHAWN RIEDEL
Correspondent
CONMED CORPORATION
14603 E. FREMONT AVE.
CENTENNIAL,  CO  80112
Correspondent Contact SHAWN RIEDEL
Regulation Number878.4400
Classification Product Code
GEI  
Date Received07/21/2006
Decision Date 01/25/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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