Device Classification Name |
Electrosurgical, Cutting & Coagulation & Accessories
|
510(k) Number |
K020186 |
Device Name |
CONMED SYSTEM 5000 ESU |
Applicant |
CONMED CORP. |
14603 E. FREMONT AVE. |
CENTENNIAL,
CO
80112
|
|
Applicant Contact |
CHARLES M (MIKE) HART |
Correspondent |
CONMED CORP. |
14603 E. FREMONT AVE. |
CENTENNIAL,
CO
80112
|
|
Correspondent Contact |
CHARLES M (MIKE) HART |
Regulation Number | 878.4400
|
Classification Product Code |
|
Date Received | 01/18/2002 |
Decision Date | 04/12/2002 |
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
|
Recalls |
CDRH Recalls
|