高级冷冻疣去除器
K号: K242288 · 2025-01-21
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器械摘要
常见问题
What is the Advanced Cryo Wart Remover?
Advanced Cryo Wart Remover is a medical device that received FDA 510(k) clearance on 2025-01-21. The listed applicant is Medical Brands Laboratories B.V.. The 510(k) number is K242288.
When did Advanced Cryo Wart Remover receive FDA 510(k) clearance?
Advanced Cryo Wart Remover received FDA 510(k) clearance on 2025-01-21, under 510(k) number K242288.
Who is the listed applicant for Advanced Cryo Wart Remover?
The FDA 510(k) record lists Medical Brands Laboratories B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Advanced Cryo Wart Remover?
The FDA product code for Advanced Cryo Wart Remover is GEH.
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Medical Brands Laboratories B.V.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:GEH)
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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