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FDA 510(k)

TROJAN SIS Synthetic Latex Condom with Silicone Lubricant

K-Number: K240379 · 2024-10-08

ApplicantChurch & Dwight Co., Inc.
Decision Date2024-10-08
Product CodeMOL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN SIS Synthetic Latex Condom with Silicone 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 2024-10-08 under 510(k) number K240379. The device is classified under product code MOL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROJAN SIS Synthetic Latex Condom with Silicone Lubricant?

TROJAN SIS Synthetic Latex Condom with Silicone Lubricant is a medical device that received FDA 510(k) clearance on 2024-10-08. The listed applicant is Church & Dwight Co., Inc.. The 510(k) number is K240379.

When did TROJAN SIS Synthetic Latex Condom with Silicone Lubricant receive FDA 510(k) clearance?

TROJAN SIS Synthetic Latex Condom with Silicone Lubricant received FDA 510(k) clearance on 2024-10-08, under 510(k) number K240379.

Who is the listed applicant for TROJAN SIS Synthetic Latex Condom with Silicone 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 SIS Synthetic Latex Condom with Silicone Lubricant?

The FDA product code for TROJAN SIS Synthetic Latex Condom with Silicone Lubricant is MOL.

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Related Devices (Code: MOL)

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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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