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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 K874851
Device Name XL-4 PAGODA (CONDOMS)
Applicant
MAYER LABORATORIES
1611 TELEGRAPH AVENUE, SUITE
830
oakland,  CA  94612
Applicant Contact david p mayer
Correspondent
MAYER LABORATORIES
1611 TELEGRAPH AVENUE, SUITE
830
oakland,  CA  94612
Correspondent Contact david p mayer
Regulation Number884.5300
Classification Product Code
HIS  
Date Received11/25/1987
Decision Date 01/21/1988
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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