Device Classification Name |
light, ultraviolet, dermatological
|
510(k) Number |
K861570 |
Device Name |
ALPHA TAN 1000 AND ALPHA TAN 1200 |
Applicant |
MIDWEST MARKETING SERVICE |
109 E. MAIN ST. |
KLEMME,
IA
50449
|
|
Applicant Contact |
NOEL KATTER |
Correspondent |
MIDWEST MARKETING SERVICE |
109 E. MAIN ST. |
KLEMME,
IA
50449
|
|
Correspondent Contact |
NOEL KATTER |
Regulation Number | 878.4630
|
Classification Product Code |
|
Date Received | 04/28/1986 |
Decision Date | 05/13/1986 |
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
|