NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOMS
K-Number: K062730 · 2006-10-05
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Device Summary
Frequently Asked Questions
What is the NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOMS?
NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOMS is a medical device that received FDA 510(k) clearance on 2006-10-05. The listed applicant is Biogreen Medical Sdn. Bhd.. The 510(k) number is K062730.
When did NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOMS receive FDA 510(k) clearance?
NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOMS received FDA 510(k) clearance on 2006-10-05, under 510(k) number K062730.
Who is the listed applicant for NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOMS?
The FDA 510(k) record lists Biogreen Medical 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 CONDOMS?
The FDA product code for NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOMS 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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