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FDA 510(k)

DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT

K-Number: K020659 · 2002-03-29

Decision Date2002-03-29
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Ssl Americas, Inc.. It received FDA 510(k) clearance on 2002-03-29 under 510(k) number K020659. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT?

DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT is a medical device that received FDA 510(k) clearance on 2002-03-29. The listed applicant is Ssl Americas, Inc.. The 510(k) number is K020659.

When did DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT receive FDA 510(k) clearance?

DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT received FDA 510(k) clearance on 2002-03-29, under 510(k) number K020659.

Who is the listed applicant for DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT?

The FDA 510(k) record lists Ssl Americas, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT?

The FDA product code for DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT is HIS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Ssl Americas, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 10 devices →

Related Devices (Code: HIS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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