CONMED HEATWAVE HAND-CONTROLLED ELETRODE


Device Classification Name

electrosurgical, cutting & coagulation & accessories

510(k) Number K021299
Device Name CONMED HEATWAVE HAND-CONTROLLED ELETRODE
Original Applicant
CONMED CORP.
525 french rd.
utica, 
NY 
13502

Original Contact ira d duesler
Regulation Number 878.4400
Classification Product Code
GEI  
Subsequent Product Code
HRX  
Date Received 04/24/2002
Decision Date 06/26/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No