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FDA 510(k)

TROJAN (TM-TBD) CONDOM

K-Number: K912901 · 1992-02-03

Decision Date1992-02-03
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN (TM-TBD) CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Carter Products. It received FDA 510(k) clearance on 1992-02-03 under 510(k) number K912901. 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-TBD) CONDOM?

TROJAN (TM-TBD) CONDOM is a medical device that received FDA 510(k) clearance on 1992-02-03. The listed applicant is Carter Products. The 510(k) number is K912901.

When did TROJAN (TM-TBD) CONDOM receive FDA 510(k) clearance?

TROJAN (TM-TBD) CONDOM received FDA 510(k) clearance on 1992-02-03, under 510(k) number K912901.

Who is the listed applicant for TROJAN (TM-TBD) CONDOM?

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

What is the FDA product code for TROJAN (TM-TBD) CONDOM?

The FDA product code for TROJAN (TM-TBD) 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 Carter Products 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 20 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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