LifeStyles NRL纹理避孕套
K号: K232279 · 2023-10-05
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决定日期2023-10-05
产品代码HIS
咨询委员会OB
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决定实质等同
器械摘要
LifeStyles NRL Textured Condom is the device name listed in this FDA 510(k) record. The listed applicant is Suretex Limited. It received FDA 510(k) clearance on 2023-10-05 under 510(k) number K232279. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LifeStyles NRL Textured Condom?
LifeStyles NRL Textured Condom is a medical device that received FDA 510(k) clearance on 2023-10-05. The listed applicant is Suretex Limited. The 510(k) number is K232279.
When did LifeStyles NRL Textured Condom receive FDA 510(k) clearance?
LifeStyles NRL Textured Condom received FDA 510(k) clearance on 2023-10-05, under 510(k) number K232279.
Who is the listed applicant for LifeStyles NRL Textured Condom?
The FDA 510(k) record lists Suretex Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LifeStyles NRL Textured Condom?
The FDA product code for LifeStyles NRL Textured Condom is HIS.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
列明Suretex Limited为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：HIS）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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