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FDA 510(k)

SteriCap 安全针头;VitreJect 安全针头

K号: K233343 · 2023-11-27

申请人Ocuject, LLC
决定日期2023-11-27
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

SteriCap Safety Needle; VitreJect Safety 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 2023-11-27 under 510(k) number K233343. 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 SteriCap Safety Needle; VitreJect Safety Needle?

SteriCap Safety Needle; VitreJect Safety Needle is a medical device that received FDA 510(k) clearance on 2023-11-27. The listed applicant is Ocuject, LLC. The 510(k) number is K233343.

When did SteriCap Safety Needle; VitreJect Safety Needle receive FDA 510(k) clearance?

SteriCap Safety Needle; VitreJect Safety Needle received FDA 510(k) clearance on 2023-11-27, under 510(k) number K233343.

Who is the listed applicant for SteriCap Safety Needle; VitreJect Safety 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 SteriCap Safety Needle; VitreJect Safety Needle?

The FDA product code for SteriCap Safety Needle; VitreJect Safety Needle is FMI.

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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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