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FDA 510(k)

MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING)

K-Number: K070830 · 2007-05-08

Decision Date2007-05-08
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING) is the device name listed in this FDA 510(k) record. The listed applicant is Karex Industries Sdn. Bhd.. It received FDA 510(k) clearance on 2007-05-08 under 510(k) number K070830. 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 MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING)?

MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING) is a medical device that received FDA 510(k) clearance on 2007-05-08. The listed applicant is Karex Industries Sdn. Bhd.. The 510(k) number is K070830.

When did MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING) receive FDA 510(k) clearance?

MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING) received FDA 510(k) clearance on 2007-05-08, under 510(k) number K070830.

Who is the listed applicant for MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING)?

The FDA 510(k) record lists Karex Industries Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING)?

The FDA product code for MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING) 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 Karex Industries Sdn. Bhd. 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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