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FDA 510(k)

DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM

K-Number: K040185 · 2004-04-27

ApplicantSsl Americas
Decision Date2004-04-27
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Ssl Americas. It received FDA 510(k) clearance on 2004-04-27 under 510(k) number K040185. 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 STUDDED/RIBBED LUBRICATED LATEX CONDOM?

DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM is a medical device that received FDA 510(k) clearance on 2004-04-27. The listed applicant is Ssl Americas. The 510(k) number is K040185.

When did DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM receive FDA 510(k) clearance?

DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM received FDA 510(k) clearance on 2004-04-27, under 510(k) number K040185.

Who is the listed applicant for DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM?

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 STUDDED/RIBBED LUBRICATED LATEX CONDOM?

The FDA product code for DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM 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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