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FDA 510(k)

Ambu USR, Ambu M

K号: K160766 · 2016-08-17

申请人Ambu A/S
决定日期2016-08-17
产品代码FAJ
咨询委员会GU
决定Substantially Equivalent

器械摘要

Ambu USR, Ambu M is the device name listed in this FDA 510(k) record. The listed applicant is Ambu A/S. It received FDA 510(k) clearance on 2016-08-17 under 510(k) number K160766. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Ambu USR, Ambu M?

Ambu USR, Ambu M is a medical device that received FDA 510(k) clearance on 2016-08-17. The listed applicant is Ambu A/S. The 510(k) number is K160766.

When did Ambu USR, Ambu M receive FDA 510(k) clearance?

Ambu USR, Ambu M received FDA 510(k) clearance on 2016-08-17, under 510(k) number K160766.

Who is the listed applicant for Ambu USR, Ambu M?

The FDA 510(k) record lists Ambu A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ambu USR, Ambu M?

The FDA product code for Ambu USR, Ambu M is FAJ.

列明Ambu A/S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:FAJ)

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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数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。

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