Device Classification Name |
pad, menstrual, unscented
|
510(k) Number |
K925250 |
Device Name |
KOTEX(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS |
Applicant |
KIMBERLY-CLARK CORP. |
700 11TH STREET, NW |
SUITE 660 |
WASHINGTON,
DC
20001
|
|
Applicant Contact |
BONNIE B WAN |
Correspondent |
KIMBERLY-CLARK CORP. |
700 11TH STREET, NW |
SUITE 660 |
WASHINGTON,
DC
20001
|
|
Correspondent Contact |
BONNIE B WAN |
Regulation Number | 884.5435
|
Classification Product Code |
|
Date Received | 10/16/1992 |
Decision Date | 03/03/1993 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Obstetrics/Gynecology
|
510k Review Panel |
Obstetrics/Gynecology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|