管清控制盒和清除茎
K号: K163092 · 2016-11-30
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器械摘要
常见问题
What is the TubeClear Control Box and Clearing Stem?
TubeClear Control Box and Clearing Stem is a medical device that received FDA 510(k) clearance on 2016-11-30. The listed applicant is Actuated Medical, Inc.. The 510(k) number is K163092.
When did TubeClear Control Box and Clearing Stem receive FDA 510(k) clearance?
TubeClear Control Box and Clearing Stem received FDA 510(k) clearance on 2016-11-30, under 510(k) number K163092.
Who is the listed applicant for TubeClear Control Box and Clearing Stem?
The FDA 510(k) record lists Actuated Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TubeClear Control Box and Clearing Stem?
The FDA product code for TubeClear Control Box and Clearing Stem is KNT.
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Actuated Medical, 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:KNT)
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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