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FDA 510(k)

THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM

K-Number: K032909 · 2003-12-16

Decision Date2003-12-16
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Thai Nippon Rubber Industry Co., Ltd.. It received FDA 510(k) clearance on 2003-12-16 under 510(k) number K032909. 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 THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM?

THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM is a medical device that received FDA 510(k) clearance on 2003-12-16. The listed applicant is Thai Nippon Rubber Industry Co., Ltd.. The 510(k) number is K032909.

When did THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM receive FDA 510(k) clearance?

THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM received FDA 510(k) clearance on 2003-12-16, under 510(k) number K032909.

Who is the listed applicant for THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM?

The FDA 510(k) record lists Thai Nippon Rubber Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM?

The FDA product code for THAI NIPPON EXTRA STRENGTH MALE LATEX 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.

Other records listing Thai Nippon Rubber Industry Co., 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.

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.

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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