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U.S. Department of Health and Human Services

510(k) Premarket Notification
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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 St., NW
Suite 660
Washington,  DC  20001
Applicant Contact BONNIE B WAN
Correspondent
Kimberly-Clark Corp.
700 11th St., NW
Suite 660
Washington,  DC  20001
Correspondent Contact BONNIE B WAN
Regulation Number884.5435
Classification Product Code
HHD  
Date Received10/16/1992
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
Predetermined Change
Control Plan Authorized		 No
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