FDA 510(k)

BD 二级输液器

K号: K223101 · 2023-05-12

决定日期2023-05-12

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

BD Secondary Infusion Set is the device name listed in this FDA 510(k) record. The listed applicant is Care Fusion. It received FDA 510(k) clearance on 2023-05-12 under 510(k) number K223101. 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 BD Secondary Infusion Set?

BD Secondary Infusion Set is a medical device that received FDA 510(k) clearance on 2023-05-12. The listed applicant is Care Fusion. The 510(k) number is K223101.

When did BD Secondary Infusion Set receive FDA 510(k) clearance?

BD Secondary Infusion Set received FDA 510(k) clearance on 2023-05-12, under 510(k) number K223101.

Who is the listed applicant for BD Secondary Infusion Set?

The FDA 510(k) record lists Care Fusion as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Secondary Infusion Set?

The FDA product code for BD Secondary Infusion Set is FPA.

列明Care Fusion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。

K233021BD SmartSite™ 13mm 瓶盖通路装置；BD SmartSite™ 20mm 瓶盖通路装置 K231888BD Texium™ 无针注射器 K221319BD Alaris® 泵硬膜外输液套装 K221327BD Alaris® 泵输液套装 K223088BD SmartSite™ 无针连接器 K223076BD Texium™ 闭式男性鲁尔接头

查看所有 14 个设备 →

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

在 FDA 数据库中查看 →

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。