Device Classification Name |
Illuminator, Fiberoptic, Surgical Field
|
510(k) Number |
K896549 |
Device Name |
STORZ FIBEROPTIC ENDO-ILLUMINATORS |
Applicant |
STORZ INSTRUMENT CO. |
3365 TREE CT. INDUSTRIAL BLVD. |
ST. LOUIS,
MO
63122 -6694
|
|
Applicant Contact |
DAN REGAN |
Correspondent |
STORZ INSTRUMENT CO. |
3365 TREE CT. INDUSTRIAL BLVD. |
ST. LOUIS,
MO
63122 -6694
|
|
Correspondent Contact |
DAN REGAN |
Regulation Number | 878.4580
|
Classification Product Code |
|
Date Received | 11/17/1989 |
Decision Date | 02/15/1990 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|