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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 K882893
Device Name CONDOMS (RAMSES, SHEIK AND KOROMEX)
Applicant
SCHMID LABORATORIES, INC.
ROUTE 46 WEST
LITTLE FALLS,  NJ  07424
Applicant Contact PHYLISS M BARBER
Correspondent
SCHMID LABORATORIES, INC.
ROUTE 46 WEST
LITTLE FALLS,  NJ  07424
Correspondent Contact PHYLISS M BARBER
Regulation Number884.5300
Classification Product Code
HIS  
Date Received07/11/1988
Decision Date 10/26/1988
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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