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FDA 510(k)

VitreJect® 注射针;OcuSafe® 注射针

K号: K230959 · 2023-09-14

申请人Ocuject, LLC
决定日期2023-09-14
产品代码FMI
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

VitreJect® Needle; OcuSafe® Needle is the device name listed in this FDA 510(k) record. The listed applicant is Ocuject, LLC. It received FDA 510(k) clearance on 2023-09-14 under 510(k) number K230959. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the VitreJect® Needle; OcuSafe® Needle?

VitreJect® Needle; OcuSafe® Needle is a medical device that received FDA 510(k) clearance on 2023-09-14. The listed applicant is Ocuject, LLC. The 510(k) number is K230959.

When did VitreJect® Needle; OcuSafe® Needle receive FDA 510(k) clearance?

VitreJect® Needle; OcuSafe® Needle received FDA 510(k) clearance on 2023-09-14, under 510(k) number K230959.

Who is the listed applicant for VitreJect® Needle; OcuSafe® Needle?

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

What is the FDA product code for VitreJect® Needle; OcuSafe® Needle?

The FDA product code for VitreJect® Needle; OcuSafe® Needle is FMI.

相关临床试验

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列明Ocuject, LLC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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相关器械(代码:FMI)

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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