Device Classification Name |
Knife, Ophthalmic
|
510(k) Number |
K863725 |
Device Name |
CATARACT DIAMOND KNIFE |
Applicant |
MEDICAL TECHNOLOGY DEVELOPMENT CORP. |
11300 49TH ST. NORTH |
CLEARWATER,
FL
33520
|
|
Applicant Contact |
JOSE H BEDOYA |
Correspondent |
MEDICAL TECHNOLOGY DEVELOPMENT CORP. |
11300 49TH ST. NORTH |
CLEARWATER,
FL
33520
|
|
Correspondent Contact |
JOSE H BEDOYA |
Regulation Number | 886.4350
|
Classification Product Code |
|
Date Received | 09/23/1986 |
Decision Date | 10/31/1986 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|