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FDA 510(k)

TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant

K-Number: K221431 · 2022-07-14

Decision Date2022-07-14
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant 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 2022-07-14 under 510(k) number K221431. 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(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant?

TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant is a medical device that received FDA 510(k) clearance on 2022-07-14. The listed applicant is Church & Dwight Co., Inc.. The 510(k) number is K221431.

When did TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant receive FDA 510(k) clearance?

TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant received FDA 510(k) clearance on 2022-07-14, under 510(k) number K221431.

Who is the listed applicant for TROJAN(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant?

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(TM) Her Pleasure Warming male natural rubber latex condom with warming lubricant?

The FDA product code for TROJAN(TM) Her Pleasure Warming male natural rubber 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 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 12 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

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