Device Classification Name |
keratome, ac-powered
|
510(k) Number |
K962661 |
Device Name |
ML MICROKERATOME BLADE |
Applicant |
MED-LOGICS, INC. |
9327 BLACKLEY ST. |
TEMPLE CITY,
CA
91780
|
|
Applicant Contact |
GLENN A DUNKIN-JACOBS |
Correspondent |
MED-LOGICS, INC. |
9327 BLACKLEY ST. |
TEMPLE CITY,
CA
91780
|
|
Correspondent Contact |
GLENN A DUNKIN-JACOBS |
Regulation Number | 886.4370
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 07/08/1996 |
Decision Date | 12/09/1996 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|