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FDA 510(k)

CONDOMS, MOODS/SHARE & RAKSHAK

K-Number: K910470 · 1991-12-18

ApplicantHindustan Latex , Ltd.
Decision Date1991-12-18
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONDOMS, MOODS/SHARE & RAKSHAK is the device name listed in this FDA 510(k) record. The listed applicant is Hindustan Latex , Ltd.. It received FDA 510(k) clearance on 1991-12-18 under 510(k) number K910470. 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 CONDOMS, MOODS/SHARE & RAKSHAK?

CONDOMS, MOODS/SHARE & RAKSHAK is a medical device that received FDA 510(k) clearance on 1991-12-18. The listed applicant is Hindustan Latex , Ltd.. The 510(k) number is K910470.

When did CONDOMS, MOODS/SHARE & RAKSHAK receive FDA 510(k) clearance?

CONDOMS, MOODS/SHARE & RAKSHAK received FDA 510(k) clearance on 1991-12-18, under 510(k) number K910470.

Who is the listed applicant for CONDOMS, MOODS/SHARE & RAKSHAK?

The FDA 510(k) record lists Hindustan Latex , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONDOMS, MOODS/SHARE & RAKSHAK?

The FDA product code for CONDOMS, MOODS/SHARE & RAKSHAK 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hindustan Latex , Ltd. 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.

K923592PATIENT EXAMINATION GLOVES

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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