Device Classification Name |
screen, tangent, projection, ac-powered
|
510(k) Number |
K914896 |
Device Name |
FRIEDMANN ANALYSER 3 |
Applicant |
CLEMENT CLARKE, INC. |
AIRMED HOUSE, EDINBURGH WAY |
HARLOW, ESSEX CM20 2ED |
ENGLAND,
GB
|
|
Applicant Contact |
MICHAEL J WILKINSON |
Correspondent |
CLEMENT CLARKE, INC. |
AIRMED HOUSE, EDINBURGH WAY |
HARLOW, ESSEX CM20 2ED |
ENGLAND,
GB
|
|
Correspondent Contact |
MICHAEL J WILKINSON |
Regulation Number | 886.1810
|
Classification Product Code |
|
Date Received | 10/31/1991 |
Decision Date | 01/23/1992 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|