一次性无菌气管插管，AccuCuff
K号: K160694 · 2017-04-07
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器械摘要
常见问题
What is the Disposable Endotracheal tube, sterile, AccuCuff?
Disposable Endotracheal tube, sterile, AccuCuff is a medical device that received FDA 510(k) clearance on 2017-04-07. The listed applicant is Tianjin Medis Medical Device Co., Ltd.. The 510(k) number is K160694.
When did Disposable Endotracheal tube, sterile, AccuCuff receive FDA 510(k) clearance?
Disposable Endotracheal tube, sterile, AccuCuff received FDA 510(k) clearance on 2017-04-07, under 510(k) number K160694.
Who is the listed applicant for Disposable Endotracheal tube, sterile, AccuCuff?
The FDA 510(k) record lists Tianjin Medis Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Disposable Endotracheal tube, sterile, AccuCuff?
The FDA product code for Disposable Endotracheal tube, sterile, AccuCuff 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Tianjin Medis Medical Device 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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