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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name condom
510(k) Number K890863
Device Name TROJAN FOR WOMEN
Applicant
ARMKEL, LLC.
HALF ACRE RD.
P.O. BOX 1001
CRANBURY,  NJ  08512
Applicant Contact C KOLAKOWSKY
Correspondent
ARMKEL, LLC.
HALF ACRE RD.
P.O. BOX 1001
CRANBURY,  NJ  08512
Correspondent Contact C KOLAKOWSKY
Regulation Number884.5300
Classification Product Code
HIS  
Date Received02/21/1989
Decision Date 04/04/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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