FDA 510(k)

一次性输尿管导引鞘

K号: K241181 · 2024-08-02

申请人Dongguan Zsr Biomedical Technology Company Limited

决定日期2024-08-02

产品代码FED

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

Disposable Ureteral Guide Sheath is the device name listed in this FDA 510(k) record. The listed applicant is Dongguan Zsr Biomedical Technology Company Limited. It received FDA 510(k) clearance on 2024-08-02 under 510(k) number K241181. The device is classified under product code FED. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Disposable Ureteral Guide Sheath?

Disposable Ureteral Guide Sheath is a medical device that received FDA 510(k) clearance on 2024-08-02. The listed applicant is Dongguan Zsr Biomedical Technology Company Limited. The 510(k) number is K241181.

When did Disposable Ureteral Guide Sheath receive FDA 510(k) clearance?

Disposable Ureteral Guide Sheath received FDA 510(k) clearance on 2024-08-02, under 510(k) number K241181.

Who is the listed applicant for Disposable Ureteral Guide Sheath?

The FDA 510(k) record lists Dongguan Zsr Biomedical Technology Company Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Ureteral Guide Sheath?

The FDA product code for Disposable Ureteral Guide Sheath is FED.

列明Dongguan Zsr Biomedical Technology Company Limited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。

K243155单次使用数字柔性输尿管镜(F-URS) (ZSR-URS-01, ZSR-URS-02, ZSR-URS-03, ZSR-URS-04)

官方来源

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