Device Classification Name |
Light, Ultraviolet, Dermatological
|
510(k) Number |
K925171 |
Device Name |
FREE SUN PRO DESIGN 3000 AND 3800 |
Applicant |
FREE SUN PROD. AB |
RASBO HAMMARBY 75596 |
UPPSALA, SWEDEN,
SE
|
|
Applicant Contact |
ERIK EKH |
Correspondent |
FREE SUN PROD. AB |
RASBO HAMMARBY 75596 |
UPPSALA, SWEDEN,
SE
|
|
Correspondent Contact |
ERIK EKH |
Regulation Number | 878.4630
|
Classification Product Code |
|
Date Received | 10/14/1992 |
Decision Date | 12/29/1992 |
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
|