Device Classification Name |
unit, phacofragmentation
|
510(k) Number |
K833800 |
Device Name |
BEECHER 20 GA. PROBE |
Applicant |
BEECHER MEDICAL DIAGNOSTIC INSTRUMENTATION |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
BEECHER MEDICAL DIAGNOSTIC INSTRUMENTATION |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 886.4670
|
Classification Product Code |
|
Date Received | 10/31/1983 |
Decision Date | 01/04/1984 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|