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FDA 510(k)

TROJAN THINTENSITY BRAND MALE LATEX CONDOM

K-Number: K071272 · 2007-09-12

Decision Date2007-09-12
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN THINTENSITY BRAND MALE LATEX CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Church & Dwight Co., Inc.. It received FDA 510(k) clearance on 2007-09-12 under 510(k) number K071272. 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 THINTENSITY BRAND MALE LATEX CONDOM?

TROJAN THINTENSITY BRAND MALE LATEX CONDOM is a medical device that received FDA 510(k) clearance on 2007-09-12. The listed applicant is Church & Dwight Co., Inc.. The 510(k) number is K071272.

When did TROJAN THINTENSITY BRAND MALE LATEX CONDOM receive FDA 510(k) clearance?

TROJAN THINTENSITY BRAND MALE LATEX CONDOM received FDA 510(k) clearance on 2007-09-12, under 510(k) number K071272.

Who is the listed applicant for TROJAN THINTENSITY BRAND MALE LATEX CONDOM?

The FDA 510(k) record lists Church & Dwight Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TROJAN THINTENSITY BRAND MALE LATEX CONDOM?

The FDA product code for TROJAN THINTENSITY BRAND MALE 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 Church & Dwight Co., 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 27 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

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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