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FDA 510(k)

TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT

K-Number: K000748 · 2000-04-06

ApplicantArmkel, LLC
Decision Date2000-04-06
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Armkel, LLC. It received FDA 510(k) clearance on 2000-04-06 under 510(k) number K000748. 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 TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT?

TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT is a medical device that received FDA 510(k) clearance on 2000-04-06. The listed applicant is Armkel, LLC. The 510(k) number is K000748.

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

TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT received FDA 510(k) clearance on 2000-04-06, under 510(k) number K000748.

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

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

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

The FDA product code for TROJAN 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 Armkel, LLC 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.

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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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