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FDA 510(k)

JOE LUBE CONDOM

K-Number: K011363 · 2002-03-25

ApplicantMarketing Sales Concepts, Inc. (Msci)
Decision Date2002-03-25
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JOE LUBE CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Marketing Sales Concepts, Inc. (Msci). It received FDA 510(k) clearance on 2002-03-25 under 510(k) number K011363. 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 JOE LUBE CONDOM?

JOE LUBE CONDOM is a medical device that received FDA 510(k) clearance on 2002-03-25. The listed applicant is Marketing Sales Concepts, Inc. (Msci). The 510(k) number is K011363.

When did JOE LUBE CONDOM receive FDA 510(k) clearance?

JOE LUBE CONDOM received FDA 510(k) clearance on 2002-03-25, under 510(k) number K011363.

Who is the listed applicant for JOE LUBE CONDOM?

The FDA 510(k) record lists Marketing Sales Concepts, Inc. (Msci) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOE LUBE CONDOM?

The FDA product code for JOE LUBE 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.

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Other records listing Marketing Sales Concepts, Inc. (Msci) 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.

K011378JOE LUB HELMET CONDOM

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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