FDA 510(k)

一次性注射针

K号: K232200 · 2024-04-12

申请人Ningbo Xinwell Medical Technology Co., Ltd.

决定日期2024-04-12

产品代码FBK

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 Injection Needles is the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Xinwell Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-04-12 under 510(k) number K232200. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Disposable Injection Needles?

Disposable Injection Needles is a medical device that received FDA 510(k) clearance on 2024-04-12. The listed applicant is Ningbo Xinwell Medical Technology Co., Ltd.. The 510(k) number is K232200.

When did Disposable Injection Needles receive FDA 510(k) clearance?

Disposable Injection Needles received FDA 510(k) clearance on 2024-04-12, under 510(k) number K232200.

Who is the listed applicant for Disposable Injection Needles?

The FDA 510(k) record lists Ningbo Xinwell Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Injection Needles?

The FDA product code for Disposable Injection Needles is FBK.

列明Ningbo Xinwell Medical Technology Co., 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。

K232969一次性止血夹

相关器械（代码：FBK）

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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