Compound W疣去除系统双功率
K号: K161294 · 2016-09-15
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决定日期2016-09-15
产品代码GEH
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Compound W Wart Removal System Dual Power is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products, Inc.. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K161294. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Compound W Wart Removal System Dual Power?
Compound W Wart Removal System Dual Power is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Medtech Products, Inc.. The 510(k) number is K161294.
When did Compound W Wart Removal System Dual Power receive FDA 510(k) clearance?
Compound W Wart Removal System Dual Power received FDA 510(k) clearance on 2016-09-15, under 510(k) number K161294.
Who is the listed applicant for Compound W Wart Removal System Dual Power?
The FDA 510(k) record lists Medtech Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Compound W Wart Removal System Dual Power?
The FDA product code for Compound W Wart Removal System Dual Power 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Medtech Products, Inc.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。
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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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