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FDA 510(k)

尼普洛 SafeTouch 针头;尼普洛 注射器和 SafeTouch 针头

K号: K222852 · 2023-05-25

决定日期2023-05-25
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

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle is the device name listed in this FDA 510(k) record. The listed applicant is Nipro Medical Corporation. It received FDA 510(k) clearance on 2023-05-25 under 510(k) number K222852. 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 Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle?

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle is a medical device that received FDA 510(k) clearance on 2023-05-25. The listed applicant is Nipro Medical Corporation. The 510(k) number is K222852.

When did Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle receive FDA 510(k) clearance?

Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle received FDA 510(k) clearance on 2023-05-25, under 510(k) number K222852.

Who is the listed applicant for Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle?

FDA 510(k)记录中列出了Nipro Medical Corporation为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle?

The FDA product code for Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle 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Nipro Medical Corporation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。

官方来源

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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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