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FDA 510(k)

ORANGE COLORED CONDOMS ORANGE SCENT

K-Number: K113056 · 2012-07-03

Decision Date2012-07-03
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ORANGE COLORED CONDOMS ORANGE SCENT 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 2012-07-03 under 510(k) number K113056. 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 ORANGE COLORED CONDOMS ORANGE SCENT?

ORANGE COLORED CONDOMS ORANGE SCENT is a medical device that received FDA 510(k) clearance on 2012-07-03. The listed applicant is Karex Industries Sdn. Bhd.. The 510(k) number is K113056.

When did ORANGE COLORED CONDOMS ORANGE SCENT receive FDA 510(k) clearance?

ORANGE COLORED CONDOMS ORANGE SCENT received FDA 510(k) clearance on 2012-07-03, under 510(k) number K113056.

Who is the listed applicant for ORANGE COLORED CONDOMS ORANGE SCENT?

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 ORANGE COLORED CONDOMS ORANGE SCENT?

The FDA product code for ORANGE COLORED CONDOMS ORANGE SCENT 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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