Carex 混合个人润滑剂
K号: K223519 · 2023-08-11
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器械摘要
常见问题
What is the Carex Hybrid Personal Lubricant?
Carex Hybrid Personal Lubricant is a medical device that received FDA 510(k) clearance on 2023-08-11. The listed applicant is Karex Industries Sdn. Bhd.. The 510(k) number is K223519.
When did Carex Hybrid Personal Lubricant receive FDA 510(k) clearance?
Carex Hybrid Personal Lubricant received FDA 510(k) clearance on 2023-08-11, under 510(k) number K223519.
Who is the listed applicant for Carex Hybrid Personal Lubricant?
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 Carex Hybrid Personal Lubricant?
The FDA product code for Carex Hybrid Personal Lubricant is NUC.
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。
相关器械(代码:NUC)
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。
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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