Device Classification Name |
perimeter, automatic, ac-powered
|
510(k) Number |
K930937 |
Device Name |
LD 400 |
Applicant |
VISMED, INC. |
10373 ROSELLE ST., SUITE 4 |
SAN DIEGO,
CA
92121
|
|
Applicant Contact |
RICH EBERHARDT |
Correspondent |
VISMED, INC. |
10373 ROSELLE ST., SUITE 4 |
SAN DIEGO,
CA
92121
|
|
Correspondent Contact |
RICH EBERHARDT |
Regulation Number | 886.1605
|
Classification Product Code |
|
Date Received | 02/23/1993 |
Decision Date | 10/18/1993 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|