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FDA 510(k)

DUREX MALE LATEX CONDOM WITH WARMING LUBRICANT

K-Number: K042957 · 2005-02-17

ApplicantSsl Americas
Decision Date2005-02-17
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DUREX MALE LATEX CONDOM WITH WARMING LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Ssl Americas. It received FDA 510(k) clearance on 2005-02-17 under 510(k) number K042957. 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 MALE LATEX CONDOM WITH WARMING LUBRICANT?

DUREX MALE LATEX CONDOM WITH WARMING LUBRICANT is a medical device that received FDA 510(k) clearance on 2005-02-17. The listed applicant is Ssl Americas. The 510(k) number is K042957.

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

DUREX MALE LATEX CONDOM WITH WARMING LUBRICANT received FDA 510(k) clearance on 2005-02-17, under 510(k) number K042957.

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

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

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

The FDA product code for DUREX MALE LATEX CONDOM WITH WARMING 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 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.

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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