Device Classification Name |
Lens, Spectacle, Non-Custom (Prescription)
|
510(k) Number |
K843096 |
Device Name |
CRISTY/COTE |
Applicant |
TITMUS OPTICAL, INC. |
PETERSBURG ,
VA
23804 -
|
|
Correspondent |
TITMUS OPTICAL, INC. |
PETERSBURG ,
VA
23804 -
|
|
Regulation Number | 886.5844
|
Classification Product Code |
|
Date Received | 08/07/1984 |
Decision Date | 11/21/1984 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|