气管插管；加固气管插管
K号: K170234 · 2018-01-17
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器械摘要
常见问题
What is the Endotracheal tube; Reinforced Endotracheal tube?
Endotracheal tube; Reinforced Endotracheal tube is a medical device that received FDA 510(k) clearance on 2018-01-17. The listed applicant is Zhanjiang Star Enterprise Co., Ltd.. The 510(k) number is K170234.
When did Endotracheal tube; Reinforced Endotracheal tube receive FDA 510(k) clearance?
Endotracheal tube; Reinforced Endotracheal tube received FDA 510(k) clearance on 2018-01-17, under 510(k) number K170234.
Who is the listed applicant for Endotracheal tube; Reinforced Endotracheal tube?
The FDA 510(k) record lists Zhanjiang Star Enterprise Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Endotracheal tube; Reinforced Endotracheal tube?
The FDA product code for Endotracheal tube; Reinforced Endotracheal tube is BTR.
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Zhanjiang Star Enterprise 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：BTR）
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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