FDA 510(k)

BD Texium™ 无针注射器

K号: K231888 · 2023-09-25

决定日期2023-09-25

产品代码FMF

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 Texium™ Needle-Free Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Care Fusion. It received FDA 510(k) clearance on 2023-09-25 under 510(k) number K231888. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD Texium™ Needle-Free Syringe?

BD Texium™ Needle-Free Syringe is a medical device that received FDA 510(k) clearance on 2023-09-25. The listed applicant is Care Fusion. The 510(k) number is K231888.

When did BD Texium™ Needle-Free Syringe receive FDA 510(k) clearance?

BD Texium™ Needle-Free Syringe received FDA 510(k) clearance on 2023-09-25, under 510(k) number K231888.

Who is the listed applicant for BD Texium™ Needle-Free Syringe?

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 Texium™ Needle-Free Syringe?

The FDA product code for BD Texium™ Needle-Free Syringe is FMF.

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 K221327BD Alaris® 泵输液套装 K221319BD Alaris® 泵硬膜外输液套装 K223101BD 二级输液器 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：FMF）

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。

K262581GraftGun® 全能移植物输送系统（GDS®）SurGenTec, LLC K252184SOL-M可更换针盘式卢埃尔锁注射器Sol-Millennium Medical, Inc.K253747一次性笔式注射器（KXYC-03C02，KXYC-03A03）Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ 安全胰岛素注射器embecta Medical II, LLC K253110Sol-Glide安全针；带注射器的Sol-Glide安全针。Sol-Millennium Medical, Inc.K260514Profoject™ 安全针；Profoject™ 带安全针的注射器；Profoject™ 低死腔注射器带安全针CMT Health PTE., Ltd.

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。