Device Classification Name |
electrosurgical, cutting & coagulation & accessories
|
510(k) Number |
K161134 |
Device Name |
Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical Generator, Bovie DERM 942 Electrosurgical Generator |
Applicant |
BOVIE MEDICAL CORPORATION |
5115 ULMERTON ROAD |
CLEARWATER,
FL
33760
|
|
Applicant Contact |
BRIAN KUNST |
Correspondent |
BOVIE MEDICAL CORPORATION |
5115 ULMERTON ROAD |
CLEARWATER,
FL
33760
|
|
Correspondent Contact |
BRIAN KUNST |
Regulation Number | 878.4400
|
Classification Product Code |
|
Date Received | 04/22/2016 |
Decision Date | 06/20/2016 |
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
|