FDA 510(k)

Scorpion Stylet门静脉通路套件，Scorpion针门静脉通路套件

K号: K202141 · 2021-01-15

决定日期2021-01-15

产品代码DYB

咨询委员会CV 请注意，由于原文未提供具体内容，以下是一个示例翻译： --- 产品名称：[产品名称] 公司名称：[公司名称] FDA批准号：[FDA批准号] 510(k)申请号：[510(k)申请号] PMA申请号：[PMA申请号] 临床试验注册号：[NCT] PubMed ID：[PMID] 产品标识符：[标识符] 产品URL：[URL] --- 请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。

决定实质等同

器械摘要

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Devices, Inc.. It received FDA 510(k) clearance on 2021-01-15 under 510(k) number K202141. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is a medical device that received FDA 510(k) clearance on 2021-01-15. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K202141.

When did Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set receive FDA 510(k) clearance?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set received FDA 510(k) clearance on 2021-01-15, under 510(k) number K202141.

Who is the listed applicant for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

The FDA 510(k) record lists Argon Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

The FDA product code for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is DYB.

列明Argon Medical Devices, 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。

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相关器械（代码：DYB）

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。

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官方来源

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