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FDA 510(k)

TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED

K-Number: K901198 · 1990-04-16

ApplicantCarter Products
Decision Date1990-04-16
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Carter Products. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K901198. 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 PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED?

TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Carter Products. The 510(k) number is K901198.

When did TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED receive FDA 510(k) clearance?

TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED received FDA 510(k) clearance on 1990-04-16, under 510(k) number K901198.

Who is the listed applicant for TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED?

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 PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED?

The FDA product code for TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED is HIS.

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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.

K955672TROJAN POLYURETHANE CONDOM (MODIFICATION)K942697TROJAN POLYURETHANE CONDOMK912901TROJAN (TM-TBD) CONDOMK904782ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TESTK904273MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB.K901202TROJAN NATURALAMB LUBRICATED NATURAL MODIFIED

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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.

K262108FAMA Male Latex Condoms – Aqueous Lubricant (Ultra-thin);FAMA Male Latex Condoms – Aqueous Lubricant (Plain);FAMA Male Latex Condoms – Aqueous Lubricant (Ribbed);FAMA Male Latex Condoms – Aqueous Lubricant (Dotted);FAMA Male Latex Condoms – Aqueous Lubricant (Non-regular Shaped);MO Male Latex Condoms – Aqueous Lubricant (Ultra-thin);MO Male Latex Condoms – Aqueous Lubricant (Plain);MO Male Latex Condoms – Aqueous Lubricant (Ribbed);MO Male Latex Condoms – Aqueous Lubricant (Dotted);MOShanghai Personage Hygiene Products Co., Ltd.K252622Male Latex Condom HAOkamoto USA, Inc.K252521LifeStyles® HydraFeel Natural Rubber Latex CondomSuretex LimitedK250034Natural rubber latex male condomShaoguan Regenex Pharmaceuticals Co., Ltd.K243421Lelo Hex Lubricated Natural Rubber Latex CondomLelo, Inc.K243640Trojan™ Ultra Ribbed Ecstasy latex condom with lubricant (Trojan™ Ultra Ribbed Ecstasy)Church & Dwight Co., Inc.

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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