FDA 510(k)

eZSURE™ 空液容器（型号426030、426040、426110）

K号: K223674 · 2023-09-01

决定日期2023-09-01

产品代码KPE

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

eZSURE™ Empty Fluid Container (models 426030, 426040, 426110) is the device name listed in this FDA 510(k) record. The listed applicant is Epic Medical Pte. , Ltd.. It received FDA 510(k) clearance on 2023-09-01 under 510(k) number K223674. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the eZSURE™ Empty Fluid Container (models 426030, 426040, 426110)?

eZSURE™ Empty Fluid Container (models 426030, 426040, 426110) is a medical device that received FDA 510(k) clearance on 2023-09-01. The listed applicant is Epic Medical Pte. , Ltd.. The 510(k) number is K223674.

When did eZSURE™ Empty Fluid Container (models 426030, 426040, 426110) receive FDA 510(k) clearance?

eZSURE™ Empty Fluid Container (models 426030, 426040, 426110) received FDA 510(k) clearance on 2023-09-01, under 510(k) number K223674.

Who is the listed applicant for eZSURE™ Empty Fluid Container (models 426030, 426040, 426110)?

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

What is the FDA product code for eZSURE™ Empty Fluid Container (models 426030, 426040, 426110)?

The FDA product code for eZSURE™ Empty Fluid Container (models 426030, 426040, 426110) is KPE.

列明Epic Medical Pte. , 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。

K252987ADRx® 混合设备 K250234SMARTeZ® 弹性输液泵（RS 系列）K251722ProSeal™ 转移注射器 (421120, 421130, 421140)K251814EZ® 静脉注射给药装置 K252094eZSURE™ 空液容器 K251340ProSeal™带添加剂端口的袋刺（423370ST，423370）

查看所有 22 个设备 →

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。