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FDA 510(k)

VACUETTE EVOPROTECT 安全血液采集/输液套装

K号: K173757 · 2018-04-19

决定日期2018-04-19
产品代码FMI
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

VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Bio-One Na, Inc.. It received FDA 510(k) clearance on 2018-04-19 under 510(k) number K173757. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set?

VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set is a medical device that received FDA 510(k) clearance on 2018-04-19. The listed applicant is Greiner Bio-One Na, Inc.. The 510(k) number is K173757.

When did VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set receive FDA 510(k) clearance?

VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set received FDA 510(k) clearance on 2018-04-19, under 510(k) number K173757.

Who is the listed applicant for VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set?

The FDA 510(k) record lists Greiner Bio-One Na, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set?

The FDA product code for VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set is FMI.

相关临床试验

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列明Greiner Bio-One Na, Inc.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。

相关器械(代码:FMI)

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。

官方来源

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