TROJAN (TM-TBD) CONDOM
K-Number: K912901 · 1992-02-03
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Device Summary
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.
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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