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FDA 510(k)

DOUBLE SPRINGERS NONOXNOL 9 CONDOM

K-Number: K012969 · 2002-06-12

ApplicantMedtech Products , Ltd.
Decision Date2002-06-12
Product CodeLTZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DOUBLE SPRINGERS NONOXNOL 9 CONDOM 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 2002-06-12 under 510(k) number K012969. The device is classified under product code LTZ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOUBLE SPRINGERS NONOXNOL 9 CONDOM?

DOUBLE SPRINGERS NONOXNOL 9 CONDOM is a medical device that received FDA 510(k) clearance on 2002-06-12. The listed applicant is Medtech Products , Ltd.. The 510(k) number is K012969.

When did DOUBLE SPRINGERS NONOXNOL 9 CONDOM receive FDA 510(k) clearance?

DOUBLE SPRINGERS NONOXNOL 9 CONDOM received FDA 510(k) clearance on 2002-06-12, under 510(k) number K012969.

Who is the listed applicant for DOUBLE SPRINGERS NONOXNOL 9 CONDOM?

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 NONOXNOL 9 CONDOM?

The FDA product code for DOUBLE SPRINGERS NONOXNOL 9 CONDOM is LTZ.

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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 RIBBEDK993733LOVE LOCKERSK993737MIGHTY MAN (DYNAMIC LINKERS)K993735DOUBLE SPRINGERS

Related Devices (Code: LTZ)

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.

K033163CAUTION CONDOMSRichard Van Haussen America, Inc.K010178SPERMICIDAL LUBRICATED MALE LATEX CONDOMInnolatex Sdn. BhdK003375CONTROL MALE CONDOMS OF NATURAL RUBBER LATEXTecnilatex S.A.K001978'ONE TOUCH' LATEX CONDOM WITH NONOXYNOL-9Thai Nippon Rubber Industry Co., Ltd.K001377SPERMICIDAL LUBRICATED MALE LATEX CONDOMPleasure Latex Products Sdn. Bhd.K992438INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT)Indus Medicare , Ltd.

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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