FDA 510(k)

Puritan Bennett Cuff Pressure Manager

K号: K202874 · 2021-01-09

决定日期2021-01-09

产品代码BSK

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决定实质等同

器械摘要

Puritan Bennett Cuff Pressure Manager is the device name listed in this FDA 510(k) record. The listed applicant is Covidien, LLC. It received FDA 510(k) clearance on 2021-01-09 under 510(k) number K202874. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Puritan Bennett Cuff Pressure Manager?

Puritan Bennett Cuff Pressure Manager is a medical device that received FDA 510(k) clearance on 2021-01-09. The listed applicant is Covidien, LLC. The 510(k) number is K202874.

When did Puritan Bennett Cuff Pressure Manager receive FDA 510(k) clearance?

Puritan Bennett Cuff Pressure Manager received FDA 510(k) clearance on 2021-01-09, under 510(k) number K202874.

Who is the listed applicant for Puritan Bennett Cuff Pressure Manager?

FDA 510(k)记录中列出Covidien, LLC为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Puritan Bennett Cuff Pressure Manager?

The FDA product code for Puritan Bennett Cuff Pressure Manager is BSK.

列明Covidien, LLC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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