FDA 510(k)

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use

K号: K221078 · 2022-11-21

申请人Sichuan Prius Biotechnology Co., Ltd.

决定日期2022-11-21

产品代码FPA

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

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Sichuan Prius Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-21 under 510(k) number K221078. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is a medical device that received FDA 510(k) clearance on 2022-11-21. The listed applicant is Sichuan Prius Biotechnology Co., Ltd.. The 510(k) number is K221078.

When did Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use receive FDA 510(k) clearance?

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use received FDA 510(k) clearance on 2022-11-21, under 510(k) number K221078.

Who is the listed applicant for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

The FDA 510(k) record lists Sichuan Prius Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

The FDA product code for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is FPA.

列明Sichuan Prius Biotechnology 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。

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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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