DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
K-Number: K020659 · 2002-03-29
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Device Summary
Frequently Asked Questions
What is the DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT?
DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT is a medical device that received FDA 510(k) clearance on 2002-03-29. The listed applicant is Ssl Americas, Inc.. The 510(k) number is K020659.
When did DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT receive FDA 510(k) clearance?
DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT received FDA 510(k) clearance on 2002-03-29, under 510(k) number K020659.
Who is the listed applicant for DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT?
The FDA 510(k) record lists Ssl Americas, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT?
The FDA product code for DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT 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 Ssl Americas, Inc. 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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