Dillard气道扩张系统
K号: K153484 · 2016-07-27
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器械摘要
常见问题
What is the Dillard Airway Dilatation System?
Dillard Airway Dilatation System is a medical device that received FDA 510(k) clearance on 2016-07-27. The listed applicant is Intuit Medical Products, LLC. The 510(k) number is K153484.
When did Dillard Airway Dilatation System receive FDA 510(k) clearance?
Dillard Airway Dilatation System received FDA 510(k) clearance on 2016-07-27, under 510(k) number K153484.
Who is the listed applicant for Dillard Airway Dilatation System?
The FDA 510(k) record lists Intuit Medical Products, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dillard Airway Dilatation System?
The FDA product code for Dillard Airway Dilatation System is KTI.
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Intuit Medical Products, LLC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:KTI)
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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