FDA 510(k)

触发开关和线缆

K号: K200455 · 2020-03-31

决定日期2020-03-31

产品代码GEI

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决定实质等同

器械摘要

Trigger Switch and Cord is the device name listed in this FDA 510(k) record. The listed applicant is New Deantronics Taiwan , Ltd.. It received FDA 510(k) clearance on 2020-03-31 under 510(k) number K200455. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Trigger Switch and Cord?

Trigger Switch and Cord is a medical device that received FDA 510(k) clearance on 2020-03-31. The listed applicant is New Deantronics Taiwan , Ltd.. The 510(k) number is K200455.

When did Trigger Switch and Cord receive FDA 510(k) clearance?

Trigger Switch and Cord received FDA 510(k) clearance on 2020-03-31, under 510(k) number K200455.

Who is the listed applicant for Trigger Switch and Cord?

The FDA 510(k) record lists New Deantronics Taiwan , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Trigger Switch and Cord?

The FDA product code for Trigger Switch and Cord is GEI.

列明New Deantronics Taiwan , 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。

查看所有 12 个设备 →

相关器械（代码：GEI）

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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