Device Classification Name |
electrode, gel, electrosurgical
|
510(k) Number |
K800933 |
Device Name |
R2 ELECTROSURG. RETURN ELECT. #225ETC. |
Applicant |
R2 CORP. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
R2 CORP. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 878.4400
|
Classification Product Code |
|
Date Received | 04/21/1980 |
Decision Date | 05/20/1980 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|