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FDA 510(k)

Bose SoundControl 听力辅助器

K号: K211008 · 2021-05-05

决定日期2021-05-05
产品代码QDD
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决定实质等同

器械摘要

Bose SoundControl Hearing Aids is the device name listed in this FDA 510(k) record. The listed applicant is Bose Corporation. It received FDA 510(k) clearance on 2021-05-05 under 510(k) number K211008. The device is classified under product code QDD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Bose SoundControl Hearing Aids?

Bose SoundControl Hearing Aids is a medical device that received FDA 510(k) clearance on 2021-05-05. The listed applicant is Bose Corporation. The 510(k) number is K211008.

When did Bose SoundControl Hearing Aids receive FDA 510(k) clearance?

Bose SoundControl Hearing Aids received FDA 510(k) clearance on 2021-05-05, under 510(k) number K211008.

Who is the listed applicant for Bose SoundControl Hearing Aids?

The FDA 510(k) record lists Bose Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bose SoundControl Hearing Aids?

The FDA product code for Bose SoundControl Hearing Aids is QDD.

相关临床试验

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。

相关器械(代码:QDD)

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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