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FDA 510(k)

TRV

K号: K192652 · 2020-05-27

决定日期2020-05-27
产品代码LXV
决定实质等同

器械摘要

TRV is the device name listed in this FDA 510(k) record. The listed applicant is Interacoustics A/S. It received FDA 510(k) clearance on 2020-05-27 under 510(k) number K192652. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

常见问题

What is the TRV?

TRV is a medical device that received FDA 510(k) clearance on 2020-05-27. The listed applicant is Interacoustics A/S. The 510(k) number is K192652.

When did TRV receive FDA 510(k) clearance?

TRV received FDA 510(k) clearance on 2020-05-27, under 510(k) number K192652.

Who is the listed applicant for TRV?

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

What is the FDA product code for TRV?

The FDA product code for TRV is LXV.

列明Interacoustics 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:LXV)

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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