Device Classification Name |
Cannula, Suction, Uterine
|
510(k) Number |
K935820 |
Device Name |
KOLSTER METHODS |
Applicant |
KOLSTER METHODS |
2550 W. ROWLAND AVE. |
ANAHEIM,
CA
92804
|
|
Applicant Contact |
ALVIN KOLSTER |
Correspondent |
KOLSTER METHODS |
2550 W. ROWLAND AVE. |
ANAHEIM,
CA
92804
|
|
Correspondent Contact |
ALVIN KOLSTER |
Regulation Number | 884.5070
|
Classification Product Code |
|
Date Received | 12/03/1993 |
Decision Date | 07/19/1994 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Obstetrics/Gynecology
|
510k Review Panel |
Obstetrics/Gynecology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|