Device Classification Name |
keratome, ac-powered
|
510(k) Number |
K980985 |
Device Name |
SCMD-1000 |
Applicant |
HOWARD INSTRUMENTS, INC. |
4749 APPLETREE LN. |
TUSCALOOSA,
AL
35405 -5747
|
|
Applicant Contact |
JACK W HOWARD |
Correspondent |
HOWARD INSTRUMENTS, INC. |
4749 APPLETREE LN. |
TUSCALOOSA,
AL
35405 -5747
|
|
Correspondent Contact |
JACK W HOWARD |
Regulation Number | 886.4370
|
Classification Product Code |
|
Date Received | 03/17/1998 |
Decision Date | 05/01/1998 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Statement |
Statement
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|