TK 导管内给药装置
K号: K191640 · 2020-08-26
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器械摘要
常见问题
What is the TK Intravascular Administration Set?
TK Intravascular Administration Set is a medical device that received FDA 510(k) clearance on 2020-08-26. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. The 510(k) number is K191640.
When did TK Intravascular Administration Set receive FDA 510(k) clearance?
TK Intravascular Administration Set received FDA 510(k) clearance on 2020-08-26, under 510(k) number K191640.
Who is the listed applicant for TK Intravascular Administration Set?
The FDA 510(k) record lists Anhui Tiankang Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TK Intravascular Administration Set?
The FDA product code for TK Intravascular Administration Set is FPA.
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Anhui Tiankang Medical Technology Co., Ltd.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:FPA)
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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