Device Classification Name |
Curette, Surgical, General Use
|
510(k) Number |
K932493 |
Device Name |
SURGICAL CURETTE |
Applicant |
WHITNEY PRODUCTS, INC. |
1822 PICKWICK LN. |
GLENVIEW,
IL
60025
|
|
Applicant Contact |
WILLIAM WHITNEY |
Correspondent |
WHITNEY PRODUCTS, INC. |
1822 PICKWICK LN. |
GLENVIEW,
IL
60025
|
|
Correspondent Contact |
WILLIAM WHITNEY |
Regulation Number | 878.4800
|
Classification Product Code |
|
Date Received | 05/24/1993 |
Decision Date | 01/07/1994 |
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
|
|
|