Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
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
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-