超视引导
K号: K251416 · 2025-12-17
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器械摘要
UltraSight Guidance is the device name listed in this FDA 510(k) record. The listed applicant is Ultrasight , Ltd.. It received FDA 510(k) clearance on 2025-12-17 under 510(k) number K251416. The device is classified under product code QJU. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the UltraSight Guidance?
UltraSight Guidance is a medical device that received FDA 510(k) clearance on 2025-12-17. The listed applicant is Ultrasight , Ltd.. The 510(k) number is K251416.
When did UltraSight Guidance receive FDA 510(k) clearance?
UltraSight Guidance received FDA 510(k) clearance on 2025-12-17, under 510(k) number K251416.
Who is the listed applicant for UltraSight Guidance?
The FDA 510(k) record lists Ultrasight , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UltraSight Guidance?
The FDA product code for UltraSight Guidance is QJU.
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Ultrasight , 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：QJU）
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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