FDA 510(k)

静脉注射输液器，静脉注射延长器

K号: K223645 · 2023-05-18

决定日期2023-05-18

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

I.V. Administration Set, I.V. Extension Set is the device name listed in this FDA 510(k) record. The listed applicant is Bq Plus Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-05-18 under 510(k) number K223645. 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 I.V. Administration Set, I.V. Extension Set?

I.V. Administration Set, I.V. Extension Set is a medical device that received FDA 510(k) clearance on 2023-05-18. The listed applicant is Bq Plus Medical Co., Ltd.. The 510(k) number is K223645.

When did I.V. Administration Set, I.V. Extension Set receive FDA 510(k) clearance?

I.V. Administration Set, I.V. Extension Set received FDA 510(k) clearance on 2023-05-18, under 510(k) number K223645.

Who is the listed applicant for I.V. Administration Set, I.V. Extension Set?

The FDA 510(k) record lists Bq Plus Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.V. Administration Set, I.V. Extension Set?

The FDA product code for I.V. Administration Set, I.V. Extension Set is FPA.

列明Bq Plus Medical 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。

K242126静脉注射输液器 K210381静脉注射输液器

相关器械（代码：FPA）

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。

K254123Ecomed 一次性给药套装Ecomed Solutions, LLC K261530iiSure 静脉输液器Deka Research and Development K252543AMSafe 注射器套装（BA-70075，BA-70071-D，BA-70070，BA-70071-P，BA-70072，BA-70072-F，BA-70071-DF，BA-70071-DF-120，FE01，FE04）Amsino International, Inc.K251375PuraCath Firefly 无针连接器 IT (9005)Puracath Medical, Inc.K251257nSet+ 稳定装置 [6426733]; nSet+ 稳定装置带 nSyte 无针连接器 (NFC) [6426731]; nSyte 无针连接器 (NFC) [6426727]Np Medical K250325BD Alaris 泵输液套装Carefusion (Bd)

官方来源

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