FDA 510(k)

泰途医疗肺音分析仪

K号: K221614 · 2023-02-24

决定日期2023-02-24

产品代码PHZ

咨询委员会AN 请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。

决定实质等同

器械摘要

TytoCare Lung Sounds Analyzer is the device name listed in this FDA 510(k) record. The listed applicant is Tyto Care , Ltd.. It received FDA 510(k) clearance on 2023-02-24 under 510(k) number K221614. The device is classified under product code PHZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the TytoCare Lung Sounds Analyzer?

TytoCare Lung Sounds Analyzer is a medical device that received FDA 510(k) clearance on 2023-02-24. The listed applicant is Tyto Care , Ltd.. The 510(k) number is K221614.

When did TytoCare Lung Sounds Analyzer receive FDA 510(k) clearance?

TytoCare Lung Sounds Analyzer received FDA 510(k) clearance on 2023-02-24, under 510(k) number K221614.

Who is the listed applicant for TytoCare Lung Sounds Analyzer?

The FDA 510(k) record lists Tyto Care , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TytoCare Lung Sounds Analyzer?

The FDA product code for TytoCare Lung Sounds Analyzer is PHZ.

列明Tyto Care , Ltd.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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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。