FDA 510(k)

TG-970P CO2 传感器套件

K号: K161860 · 2017-02-24

决定日期2017-02-24

产品代码CCK

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决定实质等同

器械摘要

TG-970P CO2 Sensor Kit is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden Corporation. It received FDA 510(k) clearance on 2017-02-24 under 510(k) number K161860. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the TG-970P CO2 Sensor Kit?

TG-970P CO2 Sensor Kit is a medical device that received FDA 510(k) clearance on 2017-02-24. The listed applicant is Nihon Kohden Corporation. The 510(k) number is K161860.

When did TG-970P CO2 Sensor Kit receive FDA 510(k) clearance?

TG-970P CO2 Sensor Kit received FDA 510(k) clearance on 2017-02-24, under 510(k) number K161860.

Who is the listed applicant for TG-970P CO2 Sensor Kit?

FDA 510(k)记录中列出Nihon Kohden Corporation为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for TG-970P CO2 Sensor Kit?

The FDA product code for TG-970P CO2 Sensor Kit is CCK.

列明Nihon Kohden Corporation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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