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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 K052206
Device Name ZEUS MALE CONDOM APPLICATOR
Applicant
CONDAX LLC.
1219 LITTLE CREEK RD.
PO BOX 12139
DURHAM,  NC  27709
Applicant Contact ELI J CARTER
Correspondent
CONDAX LLC.
1219 LITTLE CREEK RD.
PO BOX 12139
DURHAM,  NC  27709
Correspondent Contact ELI J CARTER
Regulation Number884.5300
Classification Product Code
HIS  
Date Received08/12/2005
Decision Date 09/12/2006
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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