Cook Intraosseous Infusion Needles
K号: K160887 · 2016-07-26
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器械摘要
Cook Intraosseous Infusion Needles is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2016-07-26 under 510(k) number K160887. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Cook Intraosseous Infusion Needles?
Cook Intraosseous Infusion Needles is a medical device that received FDA 510(k) clearance on 2016-07-26. The listed applicant is Cook Incorporated. The 510(k) number is K160887.
When did Cook Intraosseous Infusion Needles receive FDA 510(k) clearance?
Cook Intraosseous Infusion Needles received FDA 510(k) clearance on 2016-07-26, under 510(k) number K160887.
Who is the listed applicant for Cook Intraosseous Infusion Needles?
The FDA 510(k) record lists Cook Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cook Intraosseous Infusion Needles?
The FDA product code for Cook Intraosseous Infusion Needles is FMI.
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列明Cook Incorporated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。
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相关器械（代码：FMI）
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。
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官方来源
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