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FDA 510(k)

小型0.2mL注射器

K号: K250138 · 2025-04-02

决定日期2025-04-02
产品代码QNQ
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

Small Volume 0.2mL Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Prosum Medical Limited. It received FDA 510(k) clearance on 2025-04-02 under 510(k) number K250138. The device is classified under product code QNQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Small Volume 0.2mL Syringe?

Small Volume 0.2mL Syringe is a medical device that received FDA 510(k) clearance on 2025-04-02. The listed applicant is Prosum Medical Limited. The 510(k) number is K250138.

When did Small Volume 0.2mL Syringe receive FDA 510(k) clearance?

Small Volume 0.2mL Syringe received FDA 510(k) clearance on 2025-04-02, under 510(k) number K250138.

Who is the listed applicant for Small Volume 0.2mL Syringe?

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

What is the FDA product code for Small Volume 0.2mL Syringe?

The FDA product code for Small Volume 0.2mL Syringe is QNQ.

相关临床试验

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。

相关器械(代码:QNQ)

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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