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FDA 510(k)

LOVE GUARD MALE LATEX CONDOM

K-Number: K080833 · 2008-08-07

Decision Date2008-08-07
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LOVE GUARD MALE LATEX CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Tianjin Human-Care Latex Corporation. It received FDA 510(k) clearance on 2008-08-07 under 510(k) number K080833. 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 LOVE GUARD MALE LATEX CONDOM?

LOVE GUARD MALE LATEX CONDOM is a medical device that received FDA 510(k) clearance on 2008-08-07. The listed applicant is Tianjin Human-Care Latex Corporation. The 510(k) number is K080833.

When did LOVE GUARD MALE LATEX CONDOM receive FDA 510(k) clearance?

LOVE GUARD MALE LATEX CONDOM received FDA 510(k) clearance on 2008-08-07, under 510(k) number K080833.

Who is the listed applicant for LOVE GUARD MALE LATEX CONDOM?

The FDA 510(k) record lists Tianjin Human-Care Latex Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOVE GUARD MALE LATEX CONDOM?

The FDA product code for LOVE GUARD 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.

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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