ORANGE COLORED CONDOMS ORANGE SCENT
K-Number: K113056 · 2012-07-03
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Device Summary
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
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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