VitreJect® 注射针;OcuSafe® 注射针
K号: K230959 · 2023-09-14
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器械摘要
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
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。
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。
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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