FDA 510(k), K020659, DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
FDA 510(k), K020659, DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
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510(K) Number: K020659
Device Name: DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
Manufacturer:
Device Classification Name: Condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 03/01/2002
Decision Date: 03/29/2002
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
Manufacturer:
Device Classification Name: Condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 03/01/2002
Decision Date: 03/29/2002
Regulation Medical Specialty: Obstetrics/Gynecology