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FDA 510(k)

尿路膀胱镜

K号: K171500 · 2018-01-30

决定日期2018-01-30
产品代码FAJ
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定实质等同

器械摘要

Uro-V Cystoscope is the device name listed in this FDA 510(k) record. The listed applicant is Uroviu Corporation. It received FDA 510(k) clearance on 2018-01-30 under 510(k) number K171500. 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 Uro-V Cystoscope?

Uro-V Cystoscope is a medical device that received FDA 510(k) clearance on 2018-01-30. The listed applicant is Uroviu Corporation. The 510(k) number is K171500.

When did Uro-V Cystoscope receive FDA 510(k) clearance?

Uro-V Cystoscope received FDA 510(k) clearance on 2018-01-30, under 510(k) number K171500.

Who is the listed applicant for Uro-V Cystoscope?

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

What is the FDA product code for Uro-V Cystoscope?

The FDA product code for Uro-V Cystoscope is FAJ.

相关临床试验

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列明Uroviu Corporation为申报人的其他记录

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查看所有 7 个设备 →

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。

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