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FDA 510(k)

DOUBLE SPRINGERS

K-Number: K993735 · 2000-03-20

ApplicantMedtech Products , Ltd.
Decision Date2000-03-20
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DOUBLE SPRINGERS is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products , Ltd.. It received FDA 510(k) clearance on 2000-03-20 under 510(k) number K993735. 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 DOUBLE SPRINGERS?

DOUBLE SPRINGERS is a medical device that received FDA 510(k) clearance on 2000-03-20. The listed applicant is Medtech Products , Ltd.. The 510(k) number is K993735.

When did DOUBLE SPRINGERS receive FDA 510(k) clearance?

DOUBLE SPRINGERS received FDA 510(k) clearance on 2000-03-20, under 510(k) number K993735.

Who is the listed applicant for DOUBLE SPRINGERS?

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

What is the FDA product code for DOUBLE SPRINGERS?

The FDA product code for DOUBLE SPRINGERS 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 Medtech Products , 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.

K063401BANANA RIBBEDK012969DOUBLE SPRINGERS NONOXNOL 9 CONDOMK993733LOVE LOCKERSK993737MIGHTY MAN (DYNAMIC LINKERS)

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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