Device Classification Name |
Spectacle, Magnifying
|
510(k) Number |
K801733 |
Device Name |
FENZL RETICLE |
Applicant |
ROBERT E. FENZL, M.D. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
ROBERT E. FENZL, M.D. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 886.5840
|
Classification Product Code |
|
Date Received | 07/25/1980 |
Decision Date | 09/16/1980 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ophthalmic
|
510k Review Panel |
Ophthalmic
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|