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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 K023059
Device Name UNIDUS MALE LATEX CONDOM
Applicant
UNIDUS CORP.
1219 LITTLE CREEK RD.
DURHAM,  NC  27713
Applicant Contact ELI J CARTER
Correspondent
UNIDUS CORP.
1219 LITTLE CREEK RD.
DURHAM,  NC  27713
Correspondent Contact ELI J CARTER
Regulation Number884.5300
Classification Product Code
HIS  
Date Received09/13/2002
Decision Date 12/12/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No
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