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FDA 510(k)

TROJAN MINT TINGLE BRAND LATEX CONDOMS

K-Number: K023405 · 2002-12-16

ApplicantArmkel, LLC
Decision Date2002-12-16
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN MINT TINGLE BRAND LATEX CONDOMS is the device name listed in this FDA 510(k) record. The listed applicant is Armkel, LLC. It received FDA 510(k) clearance on 2002-12-16 under 510(k) number K023405. 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 MINT TINGLE BRAND LATEX CONDOMS?

TROJAN MINT TINGLE BRAND LATEX CONDOMS is a medical device that received FDA 510(k) clearance on 2002-12-16. The listed applicant is Armkel, LLC. The 510(k) number is K023405.

When did TROJAN MINT TINGLE BRAND LATEX CONDOMS receive FDA 510(k) clearance?

TROJAN MINT TINGLE BRAND LATEX CONDOMS received FDA 510(k) clearance on 2002-12-16, under 510(k) number K023405.

Who is the listed applicant for TROJAN MINT TINGLE BRAND LATEX CONDOMS?

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 MINT TINGLE BRAND LATEX CONDOMS?

The FDA product code for TROJAN MINT TINGLE BRAND LATEX CONDOMS 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

View on FDA Database →

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

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