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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 K052009
Device Name CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR
Applicant
CONMED CORPORATION
14603 E. FREMONT AVE.
CENTENNIAL,  CO  80112
Applicant Contact PAMELA VETTER
Correspondent
CONMED CORPORATION
14603 E. FREMONT AVE.
CENTENNIAL,  CO  80112
Correspondent Contact PAMELA VETTER
Regulation Number878.4400
Classification Product Code
GEI  
Date Received07/25/2005
Decision Date 09/28/2005
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
Recalls CDRH Recalls
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