NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM
K-Number: K023128 · 2003-01-22
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Device Summary
Frequently Asked Questions
What is the NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM?
NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM is a medical device that received FDA 510(k) clearance on 2003-01-22. The listed applicant is Secure Scientific Sdn Bhd. The 510(k) number is K023128.
When did NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM receive FDA 510(k) clearance?
NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM received FDA 510(k) clearance on 2003-01-22, under 510(k) number K023128.
Who is the listed applicant for NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM?
The FDA 510(k) record lists Secure Scientific Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM?
The FDA product code for NON-SPERMICIDAL LUBRICATED 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
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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