FDA 510(k)

IO Needle Safety Sheath

K号: K220890 · 2022-10-31

决定日期2022-10-31

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

IO Needle Safety Sheath is the device name listed in this FDA 510(k) record. The listed applicant is Actuated Medical, Inc.. It received FDA 510(k) clearance on 2022-10-31 under 510(k) number K220890. 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 IO Needle Safety Sheath?

IO Needle Safety Sheath is a medical device that received FDA 510(k) clearance on 2022-10-31. The listed applicant is Actuated Medical, Inc.. The 510(k) number is K220890.

When did IO Needle Safety Sheath receive FDA 510(k) clearance?

IO Needle Safety Sheath received FDA 510(k) clearance on 2022-10-31, under 510(k) number K220890.

Who is the listed applicant for IO Needle Safety Sheath?

The FDA 510(k) record lists Actuated Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IO Needle Safety Sheath?

The FDA product code for IO Needle Safety Sheath is FMI.

列明Actuated Medical, Inc.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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