Device Classification Name |
Refractometer, Ophthalmic
|
510(k) Number |
K890559 |
Device Name |
NIDEK AR-1200 |
Applicant |
NIDEK, INC. |
2460 EMBARCADERO WAY |
P.O.BOX 50488 |
PALO ALTO,
CA
94303
|
|
Applicant Contact |
KEN KATO |
Correspondent |
NIDEK, INC. |
2460 EMBARCADERO WAY |
P.O.BOX 50488 |
PALO ALTO,
CA
94303
|
|
Correspondent Contact |
KEN KATO |
Regulation Number | 886.1760
|
Classification Product Code |
|
Date Received | 02/06/1989 |
Decision Date | 02/27/1989 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|