扩展管
K号: K251788 · 2026-03-05
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器械摘要
常见问题
What is the Extension tube?
Extension tube is a medical device that received FDA 510(k) clearance on 2026-03-05. The listed applicant is Zhuhai DR Medical Instruments Co., Ltd.. The 510(k) number is K251788.
When did Extension tube receive FDA 510(k) clearance?
Extension tube received FDA 510(k) clearance on 2026-03-05, under 510(k) number K251788.
Who is the listed applicant for Extension tube?
The FDA 510(k) record lists Zhuhai DR Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Extension tube?
The FDA product code for Extension tube is DXT.
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Zhuhai DR Medical Instruments 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。
相关器械(代码:DXT)
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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