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FDA 510(k)

骨内注射装置

K号: K191258 · 2019-10-23

决定日期2019-10-23
产品代码FMI
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

Intraosseous infusion device is the device name listed in this FDA 510(k) record. The listed applicant is Einstein Works, LLC. It received FDA 510(k) clearance on 2019-10-23 under 510(k) number K191258. 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 Intraosseous infusion device?

Intraosseous infusion device is a medical device that received FDA 510(k) clearance on 2019-10-23. The listed applicant is Einstein Works, LLC. The 510(k) number is K191258.

When did Intraosseous infusion device receive FDA 510(k) clearance?

Intraosseous infusion device received FDA 510(k) clearance on 2019-10-23, under 510(k) number K191258.

Who is the listed applicant for Intraosseous infusion device?

The FDA 510(k) record lists Einstein Works, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intraosseous infusion device?

The FDA product code for Intraosseous infusion device is FMI.

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Einstein Works, 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: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。

官方来源

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